Thermoelectric transport in rare-earth compounds

International Nuclear Information System (INIS)

Koehler, Ulrike

2007-01-01

This work focuses on the thermoelectric transport in rare-earth compounds. The measurements of the thermal conductivity, thermopower, and Nernst coefficient are supplemented by investigations of other quantities as magnetic susceptibility and specific heat. Chapter 2 provides an introduction to the relevant physical concepts. Section 1 of that chapter summarizes the characteristic properties of rare-earth systems; section 2 gives an overview on thermoelectric transport processes in magnetic fields. The applied experimental techniques as well as the new experimental setup are described in detail in Chapter 3. The experimental results are presented in Chapter 4-6, of which each concentrates on a different subject. In Chapter 4, various Eu clathrates and the skutterudite-like Ce 3 Rh 4 Sn 13 are presented, which have been investigated as potential thermoelectric materials for applications. Chapter 5 focusses on the study of the energy scales in the heavy-fermion series Lu 1-x Yb x Rh 2 Si 2 and Ce x La 1-x Ni 2 Ge 2 by means of thermopower investigations. Chapter 6 is dedicated to the thermoelectric transport properties of the correlated semimetal CeNiSn with special emphasis on the Nernst coefficient of this compound. (orig.)

Influence of rare earth additions on the oxidation resistance of chromia forming alloys

International Nuclear Information System (INIS)

Pillis, Marina Fuser

1995-01-01

The addition of rare earths to alloys, either in elemental form or as surface coatings reduces the oxidation rate of chromia forming alloys. The rare earths either act as nucleation sites for surface oxides or get incorporates into the surface oxide and diffuse to oxide grain boundaries. If the latter occurs, a change in the defect structure close to the grain boundaries, probably takes place. In this manner, the rare earths inhibits the movement of chromium ions to the oxide/gas interface. The influence of rare earth additions to AISI 316, AISI 316L and Ni-20 Cr on their oxidation behavior has been studied., AISI 316+Ce, AISI 316+Y, Ni-20 Cr and Ni-20 Cr-2 Al-1 Ce were prepared by melting and AISI 316L, AISI 316L+Ce O 2 and AISI 316L+Y 2 O 3 by powder compaction. The effect of superficial deposits of rare earth oxides was also studied. The alloys were coated with rare earth oxides by high temperature conversion of the respective rare earth nitrates. Isothermal oxidation tests were carried out at 900-1100 deg C and the cyclic oxidation tests consisted of 6 cycles of 2 hours each at 900 deg C, followed by cooling to room temperature. All the tests were carried out in air. Oxidation behavior was evaluated gravimetrically. Scanning electron microscopy was used to study surface morphology. Energy dispersive analysis and X-ray diffraction techniques were used to identify oxide constituents. Overall, it has been observed that with the addition of rare earths, oxidation resistance increases by decreasing oxidation rates and increasing oxide adhesion. Addition of rare earths to AISI 316 prepared by melting resulted in rapid formation of a chromium rich oxide layered near the metal/oxide interface which reduced overall oxidation rate. The addition of Ce O 2 to AISI 316L was found to improve oxidation behavior after 10 hours at 1100 deg C and also inhibit the formation of volatile Cr O 3 . The isothermal oxidation behavior of rare earth oxide covered Ni-20 Cr at 900 deg C

Determination of active oxygen content in rare earth peroxides

International Nuclear Information System (INIS)

Queiroz, Carlos A.S.; Abrao, Alcidio

1993-01-01

The content of active oxygen in rare earth peroxides have been determined after the dissolution of the samples with hydrocloridic acid in the presence of potassium iodide. The free generated iodine is titrated with sodium thiosulfate using starch as indicator. The oxidation of iodide to the free iodine indicates the presence of a higher valence state rare earth oxide, until now specifically recognized for the oxides of cerium (Ce O 2 ), praseodymium (Pr 6 O 1 1) and terbium (TB 4 O 7 ). recently the authors synthesized a new series of rare earth compounds, the peroxides. These new compounds were prepared by precipitating the rare earth elements complexed with carbonate ion by addition of hydrogen peroxide. the authors demonstrated that all rare earth elements, once solubilized by complexing with carbonate ion, are quantitatively precipitated as peroxide by addition of hydrogen peroxide. (author)

Studies on the separation of rare earth elements and the nuclear decay properties of short lived rare-earth nuclides in U-235 fission products

International Nuclear Information System (INIS)

Ohyoshi, Akira; Ohyoshi, Emiko.

1980-01-01

The effect of a complex-forming agent, with which rare earths consecutively form the complexes, on the separation of a pair of adjacent rare earths by electromigration has been investigated. The relation between the separation factor for two complexes and the ligand-ion concentration was examined in the separation of La-Ce and Ce-Pr pairs with nitrilotriacetic acid. Rare earths were able to be isolated rapidly at the optimum ligand-ion concentration in lower one, and this method was applied to study the nuclear decay properties of the short lived isotopes of La, Ce, Pr, Nd and Yt formed in the fission of U-235. This method permits the direct measurement of the decay of La-144 without the interference from the radiation of other fission products. The gamma-ray spectrum of La-144 was measured with a high resolution Ge(Li) detector, and the gamma-transition was observed. From the decay plots of two strong photopeaks, the half-life of La-144 was determined. In the case of Ce fraction, the photopeaks assigned to respective isotopes were observed. In the studies on the decay properties of Pr-148 and Pr-149, the decay plot of the strong photopeak showed good linearity, and the accurate half-life of Pr-148 was determined. Similarly, the half-life of Pr-149 was longer than the previously reported value. (Kako, I.)

Thermoelectric transport in rare-earth compounds

Energy Technology Data Exchange (ETDEWEB)

Koehler, Ulrike

2007-07-01

This work focuses on the thermoelectric transport in rare-earth compounds. The measurements of the thermal conductivity, thermopower, and Nernst coefficient are supplemented by investigations of other quantities as magnetic susceptibility and specific heat. Chapter 2 provides an introduction to the relevant physical concepts. Section 1 of that chapter summarizes the characteristic properties of rare-earth systems; section 2 gives an overview on thermoelectric transport processes in magnetic fields. The applied experimental techniques as well as the new experimental setup are described in detail in Chapter 3. The experimental results are presented in Chapter 4-6, of which each concentrates on a different subject. In Chapter 4, various Eu clathrates and the skutterudite-like Ce{sub 3}Rh{sub 4}Sn{sub 13} are presented, which have been investigated as potential thermoelectric materials for applications. Chapter 5 focusses on the study of the energy scales in the heavy-fermion series Lu{sub 1-x}Yb{sub x}Rh{sub 2}Si{sub 2} and Ce{sub x}La{sub 1-x}Ni{sub 2}Ge{sub 2} by means of thermopower investigations. Chapter 6 is dedicated to the thermoelectric transport properties of the correlated semimetal CeNiSn with special emphasis on the Nernst coefficient of this compound. (orig.)

The electrorheological properties of nano-sized SiO2 particle materials doped with rare earths

International Nuclear Information System (INIS)

Liu Yang; Liao Fuhui; Li Junran; Zhang Shaohua; Chen Shumei; Wei Chenguan; Gao Song

2006-01-01

Electrorheological (ER) materials of pure SiO 2 and SiO 2 doped with rare earths (RE = Ce, Gd, Y) (non-metallic glasses (silicates)) were prepared using Na 2 SiO 3 and RECl 3 as starting materials. The electrorheological properties are not enhanced by all rare earth additions. The material doped with Ce exhibits the best ER performance

Extreme magnetoresistance in magnetic rare-earth monopnictides

Science.gov (United States)

Ye, Linda; Suzuki, Takehito; Wicker, Christina R.; Checkelsky, Joseph G.

2018-02-01

The acute sensitivity of the electrical resistance of certain systems to magnetic fields known as extreme magnetoresistance (XMR) has recently been explored in a new materials context with topological semimetals. Exemplified by WTe2 and rare-earth monopnictide La(Sb,Bi), these systems tend to be nonmagnetic, nearly compensated semimetals and represent a platform for large magnetoresistance driven by intrinsic electronic structure. Here we explore electronic transport in magnetic members of the latter family of semimetals and find that XMR is strongly modulated by magnetic order. In particular, CeSb exhibits XMR in excess of 1.6 ×106% at fields of 9 T whereas the magnetoresistance itself is nonmonotonic across the various magnetic phases and shows a transition from negative magnetoresistance to XMR with fields above magnetic ordering temperature TN. The magnitude of the XMR is larger than in other rare-earth monopnictides including the nonmagnetic members and follows a nonsaturating power law to fields above 30 T. We show that the overall response can be understood as the modulation of conductivity by the Ce orbital state and for intermediate temperatures can be characterized by an effective medium model. Comparison to the orbitally quenched compound GdBi supports the correlation of XMR with the onset of magnetic ordering and compensation and highlights the unique combination of orbital inversion and type-I magnetic ordering in CeSb in determining its large response. These findings suggest a paradigm for magneto-orbital control of XMR and are relevant to the understanding of rare-earth-based correlated topological materials.

Rare metal and rare earth pegmatites of Western India

International Nuclear Information System (INIS)

Maithani, P.B.; Nagar, R.K.

1999-01-01

Rajasthan Mica Belt in western India is one of the three major mica-producing Proterozoic pegmatite belts of India, the others being in Bihar and Andhra Pradesh. The pegmatites of these mica belts, in general, are associated with the rare metal (RM) and rare earth element (REE)-bearing minerals like columbite-tantalite, beryl, lepidolite and other multiple oxides. RM-REE pegmatites of Gujarat are devoid of commercially workable mica. These pegmatites are geologically characterised in this paper, based on their association with granite plutons geochemistry, and RM and REE potential. In addition to RM and RE-bearing pegmatites, granites of the Umedpur area, Gujarat also show anomalous concentration (0.97 wt%) of rare metals (6431 ppm Nb, 1266 ppm Ta, 454 ppm Sn, 173 ppm W), (1098 ppm Ce 1.36% Y 2 O 3 ) rare earths, and uranium (0.40% eU 3 O 8 ). Eluvial concentrations in the soil and panned concentrate (0.04-0.28 wt%) analysed up to 7.4%Nb 2 O 5 , 836 ppm Ta, and 1.31% Y. Discrete columbite-tantalite and betafite have been identified in these concentrates in addition to other minerals like zircon, rutile, sphene and xenotime. This area with discrete RM R EE mineral phases could be significant as a non-pegmatite source for rare metal and rare earths. (author)

Cerium and rare earth separation process

International Nuclear Information System (INIS)

Martin, M.; Rollat, M.

1986-01-01

An aqueous solution containing cerium III and rare earths is oxidized in the anodic compartment of an electrolytic cell, cerium IV is extracted by an organic solvent, the organic phase containing Ce IV is reduced in the catodic compartment of the same electrolytic cell and cerium III is extracted in a nitric aqueous phase [fr

Influence of rare-earth ions on fluorogallate glass formation and properties

International Nuclear Information System (INIS)

Zhang Guoyin; Poulain, M.J.

1998-01-01

Various rare earths have been incorporated in a lead fluorogallate glass with the following chemical composition: 30PbF 2 -20GaF 3 -15InF 3 -20CdF 2 -15ZnF 2 (PGICZ). Selected rare earths are La, Ce, Pr, Nd, Gd, Er, Yb and Lu, and the doping level varies between 1 and 10 mol%. The influence of rare earth fluorides on glass forming ability and on physical properties is investigated. At low concentration ( 3 in a modified PGCIZ glass have been cast. Experimental results suggest that rare earths act as modifiers rather than vitrifies in this fluorogallate system. The effect of rare earths on the values of glass transition temperature, refractive index, density and thermal expansion is reported. (orig.)

Kinetics studies of solvent extraction of rare earths into DEHPA

International Nuclear Information System (INIS)

Lim, T.M.; Tran, T.

1996-01-01

The kinetics of rare earth solvent extraction into di(2-ethylhexyl) phosphoric acid have been studied using radiotracers ( 141 Ce, 152 Eu, 153 Gd, 160 Tb and 88 Y) in a modified Lewis cell. The experimental procedure involved continuous monitoring of both aqueous and organic phases using an automated γ- counting system. Using this method, highly reproducible results were obtained without chemical analysis or disturbance of the system. The initial rate extraction was first order with respect to individual rare earth concentration. At low acidities ([H+] < 0.01 M), the extraction rates of rare earths were equal and independent of pH. However, at high acidities, the extraction rate was strongly dependent on pH and varied between the rare earths. Similarly, differences in the extraction rate of individual rare earths were apparent at low DEHPA concentration. (authors)

Distribution of rare earths in liver of mice administered with chloride compounds of 12 rare earths

International Nuclear Information System (INIS)

Shinohara, A.; Chiba, M.; Inaba, Y.

1998-01-01

Full text: Rare earths are used in high technology field, however, the information on their biological effects are not sufficient. The behaviour of rare earths in biology is of interest in connection with their toxicity. In the present study, the distribution of rare earths in liver of mice administered with these elements was investigated. The effects on Ca and other biological essential elements were also determined. Male mice (5 weeks old) were injected with one of 12 kinds of rare earths (chlorides of Y, La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er and Yb) at the dose of 25 mg/KXg body weight. After 20 hours of administration, mice were sacrificed, then liver and other organs were taken out. Liver was homogenized and separated by centrifugation. The concentrations of rare earths administered were measured by microwave-induced plasma-mass spectrometry (MIP-MS) after acid digestion. The concentrations of administered elements in whole liver were about 100μg/g (wet weight), where the difference between elements was few. Distribution amounts of elements administered in four fractions were following order; 700μg precipitate > mitocondrial fraction > microsomal fraction > cytosol. The relative contents in these fractions, however, was different depending on the element administered. Calcium concentrations in liver of administered mice were higher than those of control mice. Increase of Ca concentrations were observed in all four fractions and the increase ratio was also dependent on the elements administered

Cerium concentrate and mixed rare earth chloride by the oxidative decomposition of bastnaesite in molten sodium hydroxide

International Nuclear Information System (INIS)

Iijima, Toshio; Kato, Kazuhiro; Kuno, Toyohiko; Okuwaki, Akitsugu; Umetsu, Yoshiaki; Okabe, Taijiro

1993-01-01

Bastnaesite was treated in molten NaOH at 623-777 K for 10-60 min under atmosphere. Cerium-(III) in the ore was easily oxidized 95% or more within 30 min to give an oxidation product composed of solid solutions of CeO 2 -rich and CeO 2 -lean phases and Ce-free rare earth oxide phase. Simultaneously fluoride ion was removed 97% or more. Cerium concentrate was prepared from the oxidation product by leaching with 0.1-3 M HCl solution. The yield of cerium concentrate and the CeO 2 content reached 55-57% and 70-72%, respectively. Mixed rare earth chloride is composed of about 90% rare earth chloride and 10% alkaline earth chloride, and the contents of CeCl 3 , LaCl 3 , NdCl 3 , and PrCl 3 are 11.5, 58.5, 14.4, and 5.4%, respectively. The particle size of resulting cerium concentrate was fairly uniform and about 0.1 μm

The significant role of the rare earth ions on the elastic and thermodynamic parameters of LiCoDy- and ZnCoCe-ferrites

International Nuclear Information System (INIS)

Bishay, Samiha T.

2006-01-01

Two types of rare earth ferrites [Li 0.6 Co 0.1 Dy x Fe 2.3-x O 4 ; 0.0= 0.5 Co 0.5 Ce y Fe 2-y O 4 ; 0.0= L ) and shear (V S ) velocities, Young's modulus (E), Debye temperature (θ D ) and specific heat capacity (C v ) have been evaluated for all the investigated samples. The rare earth content as well as its ionic radius plays a significant role in the evaluated parameters. According to the experimental results, the two investigated types of rare earth ferrite are considered as insulator magnetic solids. It was found that for each composition there exists a characteristic temperature, down to which the resonance frequency of the investigated samples drops smoothly, but above this temperature the resonance frequency stays constant. Accordingly, these samples seem to be of importance in industrial applications especially in the field of electronics

Mott state and quantum critical points in rare-earth oxypnictides RO1-xFxFeAS (R= La, Sm, Nd, Pr, Ce)

NARCIS (Netherlands)

Giovannetti, G.; Kumar, S.; van den Brink, J.

2008-01-01

We investigate the magnetic phase diagram of the newly discovered iron-based high temperature oxypnictide superconductors of the type RO1-xFxFeAs, with rare earths R=La, Sm, Nd, Pr and Ce by means of ab initio SGGA and SGGA+U density functional computations. We find undoped LaOFeAs to be a Mott

Magnetism in rare-earth metals and rare-earth intermetallic compounds

International Nuclear Information System (INIS)

Johansson, B.; Nordstroem, L.; Eriksson, O.; Brooks, M.S.S.

1991-01-01

Some of out recent local spin density electronic structure calculations for a number of ferromagnetic rare-earth systems are reviewed. A simplified model of the level densities for rare-earth (R) transition metal (M) intermetallic compounds, R m M n , is used to describe in a simple way the main features of their basic electronic structure. Explicit calculations for LuFe 2 and RFe 2 (R=Gd-Yb) systems are presented, where a method to treat simultaneously the localized 4f and the conduction electron spin magnetism is introduced. Thereby it becomes possible to calculate the K RM exchange coupling constant. This method is also used to study theoretically the permanent magnet material Nd 2 Fe 14 B. The electronic structure of the anomalous ferromagnets CeFe 2 and CeCo 5 is discussed and an induced 4f itinerant magnetism is predicted. The γ-α transition in cerium metal is considered, and results from calculations including orbital polarization are presented, where a volume collapse of 10% is obtained. On one side of the transition the 4f electrons are calculated to be essentially non-bonding (localized) and on the other side they are found to contribute to the metallic bonding and this difference in behaviour gives rise to the volume collapse. Recent calculations by Wills, Eriksson and Boring for the crystal structure changes in cerium metal under high pressure are discussed. Their successful results imply an itinerant picture for the 4f electrons in α-cerium. Consequently this strongly supports the view that the γ-α phase transformation is caused by a Mott transition of the 4f electrons. (orig.)

Activation analysis of rare-earth elements in opium and cannabis samples

International Nuclear Information System (INIS)

Henke, G.

1977-01-01

Rare-earth concentrations in 65 Opium, Cannabis and Cannabis resin samples seized from various parts of the world were determined by destructive NAA. Because of the greater concentrations of Ca, P, K, Fe, Na and Si in plant materials, rare-earth elements were isolated after neutron irradiation and determined by gamma-spectrometry. The main steps of the method are: Preashing of 1 g Cannabis resin, 2.5 g Cannabis or 7.5 g Opium, respectively, in quartz ampoules (5 h, 500 deg C). Neutron irradiation, 24 h at 5x10 13 n cm -2 sec -1 . Cooling period 2-3 days. After addition of 0.1 μCi 139 Ce and rare-earth carriers wet ashing of irradiated samples with H 2 SO 4 /HNO 3 , followed by alternate addition of HNO 3 and H 2 O 2 (30%). Precipitation and removal of silicates, precipitation of fluorides, precipitation of hydroxides. Dissolution of hydroxides in HCl. Extraction with di-(2-ethylhexyl)phosphate (DEHP)/toluene and twice back-extraction of rare earths, gamma-spectrometry of HCl phase. Due to sample activity and half-life of nuclides, three measurements were made on each sample: 2 days (for La, Sm, Gd, Ho, Er, Yb); 14 days (for Nd, Lu) and 30 days after irradiation (for Ce, Eu, Tb). Great variations in absolute element concentrations, but only small significant differences of rare earth concentration ratios were found, indicating inconsiderable biogeochemical fractionation. The mean values of these ratios correspond to the relative abundances of the rare earths in the upper continental earth's crust. (T.G.)

Rare earth metals, rare earth hydrides, and rare earth oxides as thin films

International Nuclear Information System (INIS)

Gasgnier, M.

1980-01-01

The review deals with pure rare earth materials such as rare earth metals, rare earth hydrides, and rare earth oxides as thin films. Several preparation techniques, control methods, and nature of possible contaminations of thin films are described. These films can now be produced in an extremely well-known state concerning chemical composition, structure and texture. Structural, electric, magnetic, and optical properties of thin films are studied and discussed in comparison with the bulk state. The greatest contamination of metallic rare earth thin films is caused by reaction with hydrogen or with water vapour. The compound with an f.c.c. structure is the dihydride LnH 2 (Ln = lanthanides). The oxygen contamination takes place after annealing at higher temperatures. Then there appears a compound with a b.c.c. structure which is the C-type sesquioxide C-Ln 2 O 3 . At room atmosphere dihydride light rare earth thin films are converted to hydroxide Ln(OH) 3 . For heavy rare earth thin films the oxinitride LnNsub(x)Osub(y) is observed. The LnO-type compound was never seen. The present review tries to set the stage anew for the investigations to be undertaken in the future especially through the new generations of electron microscopes

Formation and decomposition of some rare earth (RE = La, Ce, Pr) hydroxides and oxides by homogeneous precipitation

International Nuclear Information System (INIS)

Ozawa, Masakuni; Onoe, Ryota; Kato, Hajime

2006-01-01

Formation and thermal decomposition of rare earth (RE = La, Ce, Pr) hydroxides and oxides by homogeneous precipitation using hexamethylenetetramine. The precipitatates were examined using thermal gravimetry and differential thermal analysis, infrared spectrometry and X-ray diffraction. The as-precipitated powders from the present process were La(OH) 3 , CeO 2 , Pr(OH) 3 . In the case of Ce, a cubic fluorite phase of cerium dioxide was directly obtained. The lanthanum trihydroxide decomposed to oxides via three steps. Two-step dehydration decomposition behavior at 340 and 500 o C was observed as La(OH) 3 → LaOOH + H 2 O and 2LaOOH → La 2 O 3 + H 2 O. The activation energy (ΔH) for dehydration was 240 and 244 kJ/mol, respectively. The additional decomposition of carbonate-containing species was observed at 670 o C with ΔH of 390 kJ/mol. Pr(OH) 3 did not show additional TGA profile of carbonate decomposition. Since no carbonate species form in solution during the HMT precipitation (hydrolysis of this molecule), the difference between La and Pr depends on the strength of basicity in the reaction with CO 2 after precipitation

Research and development of tungsten electrodes added with rare earth oxides

International Nuclear Information System (INIS)

Zuoren Nie; Ying Chen; Meiling Zhou; Tieyong Zuo

2001-01-01

The recent research and development of tungsten electrodes used in TIG and Plasma technologies are introduced, and the tungsten materials as well as the effects of rare earth oxides are specially discussed. in W-La 2 O 3 , W-CeO 2 , W-Y 2 O 3 and W-ThO 2 electrode materials, the W-2.2mass%La 2 O 3 electrode exhibited the best properties when the current is of little or middle volume, and when the electrodes are used in large current, the W-Y 2 O 3 electrode is the best. By a comparative study between the tungsten electrodes activated with single metal oxides, as above-mentioned, and those containing two or three rare earth oxides, namely La 2 O 3 , CeO 2 and Y 2 O 3 , it was indicated that the welding arc properties of the tungsten electrodes activated with combined rare earth oxides additions is superior than that of the electrodes containing single oxides as above mentioned. It was also shown that the operating properties of tungsten electrodes depend intensively on the rare earth oxides contained in the electrodes, and the actions of rare earth oxides during arcing are the most important factors to the electrodes' operating properties, temperature, work function as well as the arc stability. (author)

Replacing critical rare earth materials in high energy density magnets

Science.gov (United States)

McCallum, R. William

2012-02-01

High energy density permanent magnets are crucial to the design of internal permanent magnet motors (IPM) for hybride and electric vehicles and direct drive wind generators. Current motor designs use rare earth permanent magnets which easily meet the performance goals, however, the rising concerns over cost and foreign control of the current supply of rare earth resources has motivated a search for non-rare earth based permanent magnets alloys with performance metrics which allow the design of permanent magnet motors and generators without rare earth magnets. This talk will discuss the state of non-rare-earth permanent magnets and efforts to both improve the current materials and find new materials. These efforts combine first principles calculations and meso-scale magnetic modeling with advance characterization and synthesis techniques in order to advance the state of the art in non rare earth permanent magnets. The use of genetic algorithms in first principle structural calculations, combinatorial synthesis in the experimental search for materials, atom probe microscopy to characterize grain boundaries on the atomic level, and other state of the art techniques will be discussed. In addition the possibility of replacing critical rare earth elements with the most abundant rare earth Ce will be discussed.

Strong broad green UV-excited photoluminescence in rare earth (RE = Ce, Eu, Dy, Er, Yb) doped barium zirconate

Energy Technology Data Exchange (ETDEWEB)

Borja-Urby, R. [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico); Diaz-Torres, L.A., E-mail: ditlacio@cio.mx [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico); Salas, P. [Centro de Fisica Aplicada y Tecnologia Avanzada, Universidad Nacional Autonoma de Mexico, A.P. 1-1010, Queretaro, Qro. 76000 (Mexico); Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Ciudad de Mexico, D. F. 07730 (Mexico); Meza, O. [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico)

2011-10-25

Highlights: > Trivalent rare earth (RE) substitution on Zr{sup 4+} sites in BaZrO{sub 3} lead to band gap narrowing. > RE substitution lead to enhanced blue-green intrinsic emission of nanocrystalline BaZrO{sub 3} > Blue-green hue of BaZrO3:RE depends on RE dopant and excitation UV wavelength > BaZrO3: Dy{sup 3+} PL chromatic coordinates correspond to pure white color coordinates of CIE 1931 model - Abstract: The wet synthesis hydrothermal method at 100 deg. C was used to elaborate barium zirconate (BaZrO{sub 3}) unpurified with 0.5 mol% of different rare earth ions (RE = Yb, Er, Dy, Eu, Ce). Morphological, structural and UV-photoluminescence properties depend on the substituted rare earth ionic radii. While the crystalline structure of RE doped BaZrO{sub 3} remains as a cubic perovskite for all substituted RE ions, its band gap changes between 4.65 and 4.93 eV. Under 267 nm excitation the intrinsic green photoluminescence of the as synthesized BaZrO{sub 3}: RE samples is considerably improved by the substitution on RE ions. For 1000 deg. C annealed samples, under 267 nm, the photoluminescence is dominated by the intrinsic BZO emission. It is interesting to notice that Dy{sup 3+}, Er{sup 3+} and Yb{sup 3+} doped samples present whitish emissions that might be useful for white light generation under 267 nm excitation. CIE color coordinates are reported for all samples.

Recovery and purification of rare earth elements and thorium

International Nuclear Information System (INIS)

Sungur, A.; Saygi, Z.; Yildiz, H.

1985-01-01

Rare earth elements and thorium found in the low-grade Eskisehir-Beylikahir ore have been recovered by HCl leaching, Lanthanides and thorium were separated and purified from the leach solutions through the precipitation sequence as double sulphate, hydroxide and oxalate. The Ln 2 O 3 and Th(OH) 4 products, finally obtained contained 36% Ce and 65% Th. The analysis of rare earth elements, thorium and other present ingredients were carried out by instrumental neutron activation analysis, atomic absorption spectroscopy, vis-spectroscopy and gravimetry. (author)

Determination Of Rare Earth And Other Elements In YEN-PHU Rare Earth Ore And Other Intermediate Products From The Floatation And Hydrometallurgical Process On Portable XRF Si-PIN Detector

International Nuclear Information System (INIS)

Doan Thanh Son; Phung Vu Phong; Nguyen Hanh Phuc

2014-01-01

The concentration of rare earths elements such as La, Ce, Pr, Nd, Gd and other elements as Ca, Fe, U, Th in Yen Phu rare earth ore and other intermediate products from the flotation and hydrometallurgical process was determined by using Si-PIN detector fluorescence spectrometry. The precision and accuracy of quantitative analysis was tested by standard reference materials and comparative analysis with different analytical methods. The analytical procedures were set-up and applied for the determination of rare earth and other elements in Yen Phu rare earth ore and other intermediate products from the flotation and hydrometallurgical process with high precision and accuracy. (author)

Investigations on fabricating strategies and utilization of rare earth based multicomponent oxide powders in radiation detection

International Nuclear Information System (INIS)

Shinde, Seema; Pitale, S.S.; Banthia, S.; Ghosh, M.; Tyagi, M.; Sen, S.; Gadkari, S.C.

2014-01-01

Materials containing rare earths demonstrate a broad field of applications as high energy radiation detectors, mainly due to their fascinating optical properties. Currently, Ce 3+ -doped rare earth silicates and garnets dominate the scintillator market because they show a high light yield, fast decay time, and high chemical stability. Moreover, the emission wavelength of silicates (410-440 nm) matches the wavelength sensitivity of conventional PMTs while, Si-photo-detector readouts are possible with garnets (emission near 550 nm). The composition, structure and phase of rare earth silicates are rather complex. For example, there are many phases like oxyorthosilicate R 2 SiO 5 , disilicate R 2 Si 2 O 7 , hexagonal R x (SiO 4 ) 6 O 2 oxyapatite etc (where R= Rare earth element). The controlled synthesis of single phase rare earth silicates and garnets nanomaterials is not easy and can only be reached with precisely controlled experimental conditions. In this work, we provide a broad overview of our recent scientific developments linked to a few aspects of synthesizing cerium activated rare earth based silicates and garnet materials, namely Gd 2 SiO 5 :Ce 3+ , Gd 4.67 (SiO 4 ) 3 O, Gd 2 Si 2 O 7 :Ce 3+ and Gd 3 Al x Ga 1-x O 12 :Ce 3+ (where 0≤x≤5) exploiting the advantages of solution combustion, chemical co-precipitation and hydrothermal techniques. A brief summary of results based on synthesis strategy adopted, composition, size shape and corresponding luminescence features of Gd based compounds are tabulated. The room temperature photoluminescence (PL) features of compounds listed. Efforts towards finding new properties and new materials will be continued and several applications, in particular energy-conversion and scintillator detectors, will benefit from these rare earth materials

Preparation and characteristics of various rare earth nitrides

International Nuclear Information System (INIS)

Imamura, H.; Imahashi, T.; Zaimi, M.; Sakata, Y.

2008-01-01

Active nanocrystalline nitrides of EuN and YbN with high surface areas were successfully prepared by the thermal decomposition of the rare earth amides (Eu(NH 2 ) 2 , Yb(NH 2 ) 2 and Yb(NH 2 ) 3 ). For the preparation of CeN, PrN and NdN, the direct reaction of the rare earth metals with ammonia was extensively studied to determine optimal conditions. In the reaction of rare earth metals with ammonia, hydrides besides the nitrides were competitively formed. The reaction conditions such as temperatures and ratios of ammonia to rare earth metal were crucial in preferential formation of nitride. The nanocrystalline YbN and EuN readily absorbed large amounts of ammonia even at room temperature upon contact with ammonia (13.3 kPa). The absorbed ammonia existed in at least two forms on/in the nitride; the one was surface-adsorbed ammonia and the other ammonia absorbed in the nitride in a decomposed state. The properties of ammonia absorbed by the nitride were further evaluated by temperature-programmed desorption (TPD), FT-IR and XRD techniques

Spectrofluorimetric characterization and study for the determination of rare earth carbonate complexes

International Nuclear Information System (INIS)

Dantas, E.S.K.; Abrao, A.

1982-01-01

Some rare earths exhibit fluorescence in acid solution (HC1, H 2 SO 4 or HC10 4 ) when irradiated with ultraviolet radiation; however, analytical application of this property has not been proposed due to the lack of sensitivity resulted from the weakness of the fluorescence transitions. The rare earths are soluble in alkali carbonate solutions, forming anionic carbonate complexes (TR(CO 3 ) sup(n-) sub(x)); some of them have stronger absorption bands than those obtained in acid media. Using this property, the characterization and determination of the six rare earths which fluoresce in carbonate solution has been studied. The excitation and emission wavelengths are (in nm): Sm (406, 596); Eu (280,612); Gd (272,312); Tb (240,542); Dy (350, 576) and Tm (360, 450). Although Ce-III is highly fluorescent in acid media, when in carbonate solution it is easily oxidized to Ce-IV which does not fluoresce neither in acid nor in carbonate solutions. The other rare earths, although soluble in carbonate solution, do not fluoresce in this medium. A comparison is made, between the fluorescence of the fluorescing lanthanides, in acid and carbonate media. The precision and accuracy of this method, the detection limit of all rare earths studied and the mutual interference of some of them is also discussed. The method will be applied to the analytical control of the separation and purification of individual rare earths, now under development. (Author) [pt

Solvent extraction of uranium, thorium, and rare earths with dialkyldithiophosphoric acids

International Nuclear Information System (INIS)

Haiduc, I.; Curtui, M.

1986-01-01

The separation conditions for throium (IV) in the presence of trivalent rare earths was investigated. The distribution ratios (D), extraction effectivity values (E%) and separation factor(S) were calculated for binary systems Th-La, Th-Ce, Th-Pr, Th-Sm. Di-(2-ethyl-hexyl)dithiophosphoric acid (HEhdtp) alone or mixtures of HEhdtp and trioctylphosphoshine oxide (TOPO) can be successfully used for separation of Thorium (IV) and rare earths

Neutron activation analysis of rare earths in uranium containing rocks

International Nuclear Information System (INIS)

May, S.; Pinte, G.

1984-01-01

The determination of rare earths by activation analysis in uranium rocks is disturbed either by fission-produced rare earths, or by neptunium-239 originating from uranium-238. In order to eliminate these interferencies, the chemical separation of rare earths from uranium prior to activation should be performed. The chemical process is as follows: the rock sample is fused with sodium borate, then, after addition of hydrochloric acid, the resulting solution is passed through a Dowex 1x8 column. Uranium is retained on the resin, and rare earths and scandium are eluted. Aluminium is added as a carrier to the solution, and rare earths and scandium are coprecipitated with aluminium hydroxide. This precipitate is irradiated in the nuclear reactor. Gamma spectrometry is used for the determination of earth radionuclide. Activity measurements are performed in successive steps during one month. The following elements are determined: Pr, La, Sm, Nd, Yb, Lu, Ce, Tb, Eu and Sc. The chemical yield is measured by using scandium as an internal standard. (author)

Rare earth niobate coordination polymers

Science.gov (United States)

Muniz, Collin N.; Patel, Hiral; Fast, Dylan B.; Rohwer, Lauren E. S.; Reinheimer, Eric W.; Dolgos, Michelle; Graham, Matt W.; Nyman, May

2018-03-01

Rare-earth (RE) coordination polymers are infinitely tailorable to yield luminescent materials for various applications. Here we described the synthesis of a heterometallic rare-earth coordination compound ((CH3)2SO)3(RE)NbO(C2O4)3((CH3)2SO) = dimethylsulfoxide, DMSO, (C2O2= oxalate), (RE=La, Ce, Pr, Nd, Sm, Eu, Gd, Tb). The structure was obtained from single crystal X-ray diffraction of the La analogue. The Nb˭O and DMSO terminal-bonding character guides assembly of an open framework structure with noncentrosymmetric RE-coordination geometry, and large spacing between the RE centers. A second structure was observed by PXRD for the smaller rare earths (Dy, Ho, Er, Yb); this structure has not yet been determined. The materials were further characterized using FTIR, and photoluminescence measurements. Characteristic excitation and emission transitions were observed for RE = Nd, Sm, Eu, and Tb. Quantum yield (QY) measurements were performed by exciting Eu and Tb analoges at 394 nm (QY 66%) and 464 nm (QY 71%) for Eu; and 370 nm (QY=40%) for Tb. We attribute the high QY and bright luminescence to two main structure-function properties of the system; namely the absence of water in the structure, and absence of concentration quenching.

Effect of Rare Earth Metals on the Microstructure of Al-Si Based Alloys

Directory of Open Access Journals (Sweden)

Saleh A. Alkahtani

2016-01-01

Full Text Available The present study was performed on A356 alloy [Al-7 wt %Si 0.0.35 wt %Mg]. To that La and Ce were added individually or combined up to 1.5 wt % each. The results show that these rare earth elements affect only the alloy melting temperature with no marked change in the temperature of Al-Si eutectic precipitation. Additionally, rare earth metals have no modification effect up to 1.5 wt %. In addition, La and Ce tend to react with Sr leading to modification degradation. In order to achieve noticeable modification of eutectic Si particles, the concentration of rare earth metals should exceed 1.5 wt %, which simultaneously results in the precipitation of a fairly large volume fraction of insoluble intermetallics. The precipitation of these complex intermetallics is expected to have a negative effect on the alloy performance.

A Novel Synthesis Routine for Woodwardite and Its Affinity towards Light (La, Ce, Nd and Heavy (Gd and Y Rare Earth Elements

Directory of Open Access Journals (Sweden)

Sirio Consani

2018-01-01

Full Text Available A synthetic Cu-Al-SO4 layered double hydroxide (LDH, analogue to the mineral woodwardite [Cu1−xAlx(SO4x/2(OH2·nH2O], with x < 0.5 and n ≤ 3x/2, was synthesised by adding a solution of Cu and Al sulphates to a solution with NaOH. The pH values were kept constant at 8.0 and 10.0 by a continuous addition of NaOH. The material obtained had poor crystallinity, turbostratic structure, and consisted of nanoscopic crystallites. The analyses performed in order to characterise the obtained materials (X-ray diffraction (XRD, thermogravimetry (TG, and Fourier Transform Infra-Red (FTIR spectroscopy showed that the Cu-Al-SO4 LDH is very similar to woodwardite, although it has a smaller layer spacing, presumably due to a lesser water content than in natural samples. The synthesis was performed by adding light rare earth elements (LREEs (La, Ce, and Nd and heavy rare earth elements (HREEs (Gd and Y in order to test the affinity of the Cu-Al-SO4 LDH to the incorporation of REEs. The concentration of rare earth elements (REEs in the solid fraction was in the range of 3.5–8 wt %. The results showed a good affinity for HREE and Nd, especially for materials synthesised at pH 10.0, whereas the affinities for Ce and La were much lower or non-existent. The thermal decomposition of the REE-doped materials generates a mixture of Cu, Al, and REE oxides, making them interesting as precursors in REE oxide synthesis.

Formation and decomposition of some rare earth (RE = La, Ce, Pr) hydroxides and oxides by homogeneous precipitation

Energy Technology Data Exchange (ETDEWEB)

Ozawa, Masakuni [Ceramics Research Laboratory, Nagoya Institute of Technology, Tajimi, 507-0071 Gifu (Japan)]. E-mail: ozawa@crl.nitech.ac.jp; Onoe, Ryota [Ceramics Research Laboratory, Nagoya Institute of Technology, Tajimi, 507-0071 Gifu (Japan); Kato, Hajime [Ceramics Research Laboratory, Nagoya Institute of Technology, Tajimi, 507-0071 Gifu (Japan)

2006-02-09

Formation and thermal decomposition of rare earth (RE = La, Ce, Pr) hydroxides and oxides by homogeneous precipitation using hexamethylenetetramine. The precipitatates were examined using thermal gravimetry and differential thermal analysis, infrared spectrometry and X-ray diffraction. The as-precipitated powders from the present process were La(OH){sub 3}, CeO{sub 2}, Pr(OH){sub 3}. In the case of Ce, a cubic fluorite phase of cerium dioxide was directly obtained. The lanthanum trihydroxide decomposed to oxides via three steps. Two-step dehydration decomposition behavior at 340 and 500 {sup o}C was observed as La(OH){sub 3} {sup {yields}} LaOOH + H{sub 2}O and 2LaOOH {sup {yields}} La{sub 2}O{sub 3} + H{sub 2}O. The activation energy ({delta}H) for dehydration was 240 and 244 kJ/mol, respectively. The additional decomposition of carbonate-containing species was observed at 670 {sup o}C with {delta}H of 390 kJ/mol. Pr(OH){sub 3} did not show additional TGA profile of carbonate decomposition. Since no carbonate species form in solution during the HMT precipitation (hydrolysis of this molecule), the difference between La and Pr depends on the strength of basicity in the reaction with CO{sub 2} after precipitation.

Prospecting and exploration of rare earth bearing mineral resources in India: an overview

International Nuclear Information System (INIS)

Mohanty, R.

2014-01-01

Rare earth elements (REE) have a wide range of applications including nuclear and the REE bearing minerals occur in varied geological environments.The commercial rare earth bearing minerals are monazite ((Ce,La,Pr,Nd,Th,Y)PO 4 ), xenotime (YPO 4 ), bastnasite ((Ce,La,Y)CO 3 F) and pyrochlore ((Na,Ca) 2 Nb 2 O 6 (OH,F) which occur either as placer concentrations or in tracer quantities in rocks. While Monazite contains dominantly LREE, Xenotime and Bastnasite are richer in HREE. The exploration and evaluation of these two types of occurrences follow different methodologies

Rare earths

Energy Technology Data Exchange (ETDEWEB)

Cranstone, D A

1979-01-01

Rare earth elements are commonly extracted from the minerals monazite, bastnaesite, and xenotine. New uses for these elements are constantly developing; they have found applications in glass polishing, television tube phosphors, high-strength low-alloy steels, magnets, catalysts, refractory ceramics, and hydrogen sponge alloys. In Canada, rare earths have been produced as byproducts of the uranium mining industry, but there was no production of rare earths in 1978 or 1979. The world sources of and markets for the rare earth elements are discussed.

Dissolved rare earth elements in the Black Sea

NARCIS (Netherlands)

Schijf, Johan; Baar, Hein J.W. de; Wijbrans, Jan R.; Landing, William M.

1991-01-01

Concentrations of rare earths in the deep anoxic Black Sea are about one order of magnitude higher than in normal open ocean waters. From a minimum at the suboxic-anoxic interface at about 107 m depth, concentrations increase strongly to a maximum at about 300–400 m depth. Concentrations of Ce range

Ternary rare earth sulfide CaCe2S4: Synthesis and characterization of stability, structure, and photoelectrochemical properties in aqueous media

Science.gov (United States)

Sotelo, Paola; Orr, Melissa; Galante, Miguel Tayar; Hossain, Mohammad Kabir; Firouzan, Farinaz; Vali, Abbas; Li, Jun; Subramanian, Mas; Longo, Claudia; Rajeshwar, Krishnan; Macaluso, Robin T.

2018-06-01

A red-orange rare earth ternary chalcogenide, CaCe2S4, was prepared in powder form by solid-state synthesis. The structural details of this compound were determined by powder X-ray diffraction. The optical band gap of CaCe2S4 was determined by diffuse reflectance spectroscopy (DRS) to be 2.1 eV, consistent with the observed red-orange color. Quantitative colorimetry measurements also support the observed color and band gap of CaCe2S4. Both direct and indirect optical transitions were gleaned from Tauc analyses of the DRS data. Photoelectrochemistry experiments on CaCe2S4 films showed n-type semiconductor behavior. Analyses of these data via the Butler-Gärtner model afforded a flat-band potential of - 0.33 V (vs. Ag/AgCl/KCl 4 M) in pH 9 aqueous sulfite electrolyte. The potential and limitations of this material for solar water splitting and photocatalytic environmental remediation (e.g., dye photodegradation) are finally presented against the backdrop of its photoelectrochemical stability and surface hole transfer kinetics in aqueous electrolytes.

Concentration of light rare earths process by amoniacal precipitation

International Nuclear Information System (INIS)

Aguilera, Y.; Rapado, M.; Consuegra, R.

1996-01-01

A procedure for the separation and concentration of light rare earths using a mixture of ammonia and water was developed. As a result technical concentrates of rare earths were obtained and the physical separation in the filtration step was improved. The filtration parameters (cake resistance r 0 and filtration web resistance R) were obtained for this process being they 5,5.10 11 cm/g and 3,4.10 13 cm -1 respectively. The proposed technology concentrates (Ce, La and Nd) with purities ranging from: 85-90 %, 85-87 % and 42-65 % respectively in only one precipitation step

Study on recovering directly the commercial cerium oxide and total of residue rare earths from Dongpao bastnasite concentrate

International Nuclear Information System (INIS)

Nguyen Trong Hung; Nguyen Thanh Chung; Luu Xuan Dinh

2003-01-01

A technology for decomposition roasting and sequential leaching processes of Dong Pao bastnasite concentrate to recover directly commercial cerium oxide and total of residue rare earth elements from the leaching solution of the roasted product have been investigated. The bastnasite concentrate is initially roasted at temperature range of 600 - 650 degC and for time of 4 hrs in order to decompose and convert the hardly soluble carbonate forms of ore into easily soluble oxide. The roasted solid is then leached with sulfuric acid solution of 6N at 60 degC for 4 hrs to convert rare earths in oxide and fluoride form into rare earth sulfate. The recovery yield of rare earths of these stages is more than 95%. The attention has especially been paid on recovering directly the commercial cerium oxide and total of residue rare earth element from the above leaching solution. Complex ions of CeSO 4 2+ , Ce(SO 4 ) 2 , Ce(SO 4 ) 3 2- and Ce(SO 4 ) 4 4- exist in aqueous solution of cerium (IV) sulfate. Based on the property, the method of ion - sieve with DOWEX cation resin column has been applied to estimating separation of the ceric complex anions from Ln(III). The survey showed that most of the ceric complex anions are separated from total of residue rare earths. The latter which are absorbed in the cation column are recovered by elution of HCl of 4N. The recovery yield of cerium can only be reached 20% but the purity of that is very high, can be reached 99.6%. About 5 kg of CeO 2 of high grade and 5 kg of TREO of commercial specification have been produced. (author)

Comparative study of rare earth hexaborides using high resolution angle-resolved photoemission

Energy Technology Data Exchange (ETDEWEB)

Ramankutty, S.V., E-mail: s.v.ramankutty@uva.nl [Van der Waals-Zeeman Institute, Institute of Physics (IoP), University of Amsterdam, Science Park 904, 1098 XH Amsterdam (Netherlands); Jong, N. de; Huang, Y.K.; Zwartsenberg, B. [Van der Waals-Zeeman Institute, Institute of Physics (IoP), University of Amsterdam, Science Park 904, 1098 XH Amsterdam (Netherlands); Massee, F. [Laboratory of Atomic and Solid State Physics, Department of Physics, Cornell University, Ithaca, NY 14853 (United States); Bay, T.V. [Van der Waals-Zeeman Institute, Institute of Physics (IoP), University of Amsterdam, Science Park 904, 1098 XH Amsterdam (Netherlands); Golden, M.S., E-mail: m.s.golden@uva.nl [Van der Waals-Zeeman Institute, Institute of Physics (IoP), University of Amsterdam, Science Park 904, 1098 XH Amsterdam (Netherlands); Frantzeskakis, E., E-mail: e.frantzeskakis@uva.nl [Van der Waals-Zeeman Institute, Institute of Physics (IoP), University of Amsterdam, Science Park 904, 1098 XH Amsterdam (Netherlands)

2016-04-15

Highlights: • ARPES electronic structure study of rare-earth (RE) hexaborides SmB{sub 6}, CeB{sub 6} and YbB{sub 6}. • Increasing RE valence Yb[II], Sm[II/III], Ce[III] increases d-band occupancy. • YbB{sub 6} and SmB{sub 6} posses 2D states at E{sub F}, whereas the Fermi surface of CeB{sub 6} is 3D. • ARPES, LEED and STM data prove structural relaxation of the SmB{sub 6}(001) surface. - Abstract: Strong electron correlations in rare earth hexaborides can give rise to a variety of interesting phenomena like ferromagnetism, Kondo hybridization, mixed valence, superconductivity and possibly topological characteristics. The theoretical prediction of topological properties in SmB{sub 6} and YbB{sub 6} has rekindled the scientific interest in the rare earth hexaborides, and high-resolution ARPES has been playing a major role in the debate. The electronic band structure of the hexaborides contains the key to understand the origin of the different phenomena observed, and much can be learned by comparing the experimental data from different rare earth hexaborides. We have performed high-resolution ARPES on the (001) surfaces of YbB{sub 6}, CeB{sub 6} and SmB{sub 6}. On the most basic level, the data show that the differences in the valence of the rare earth element are reflected in the experimental electronic band structure primarily as a rigid shift of the energy position of the metal 5d states with respect to the Fermi level. Although the overall shape of the d-derived Fermi surface contours remains the same, we report differences in the dimensionality of these states between the compounds studied. Moreover, the spectroscopic fingerprint of the 4f states also reveals considerable differences that are related to their coherence and the strength of the d–f hybridization. For the SmB{sub 6} case, we use ARPES in combination with STM imaging and electron diffraction to reveal time dependent changes in the structural symmetry of the highly debated SmB{sub 6

141Ce as a tracer to find the efficient washing method for hair in the analysis of rare earth elements

International Nuclear Information System (INIS)

Tong Shilu

1989-01-01

Various procedures were compared in relation to the removal of 141 Ce exogenously contaminated as well as endogenously incorporated in hair. Extraction efficiency of cerium with hot EDTA was the greatest among the four washing procedures. However, no procedure can effectively remove all exogenous cerium without reducing the endogenous cerium. Among the four procedures evaluated, washing with 0.1 mol/l EDTA (50 deg C, 10 minutes) is recommended before the analysis of rare earth elements in hair because of its efficiency in removing exogenous cerium and causing less loss on endogenous cerium

Rare earth germanates

International Nuclear Information System (INIS)

Bondar', I.A.; Vinogradova, N.V.; Dem'yanets, L.N.

1983-01-01

Rare earth germanates attract close attention both as an independent class of compounds and analogues of a widely spread class of natural and synthetic minerals. The methods of rare earth germanate synthesis (solid-phase, hydrothermal) are considered. Systems on the basis of germanium and rare earth oxides, phase diagrams, phase transformations are studied. Using different chemical analysese the processes of rare earth germanate formation are investigated. IR spectra of alkali and rare earth metal germanates are presented, their comparative analysis being carried out. Crystal structures of the compounds, lattice parameters are studied. Fields of possible application of rare earth germanates are shown

Rare earth elements recycling from waste phosphor by dual hydrochloric acid dissolution

International Nuclear Information System (INIS)

Liu, Hu; Zhang, Shengen; Pan, Dean; Tian, Jianjun; Yang, Min; Wu, Maolin; Volinsky, Alex A.

2014-01-01

Highlights: • The article provides a new method for recycling rare earth (RE) from waste phosphor. • When compared with the traditional methods, leach rate was much higher. • Y–Eu concentrate and Tb–Ce concentrate were obtained successively. • It would reduce the burden of later extraction, separation and purification. - Abstract: This paper is a comparative study of recycling rare earth elements from waste phosphor, which focuses on the leaching rate and the technical principle. The traditional and dual dissolution by hydrochloric acid (DHA) methods were compared. The method of dual dissolution by hydrochloric acid has been developed. The Red rare earth phosphor (Y 0.95 Eu 0.05 ) 2 O 3 in waste phosphor is dissolved during the first step of acid leaching, while the Green phosphor (Ce 0.67 Tb 0.33 MgAl 11 O 19 ) and the Blue phosphor (Ba 0.9 Eu 0.1 MgAl 10 O 17 ) mixed with caustic soda are obtained by alkali sintering. The excess caustic soda and NaAlO 2 are removed by washing. The insoluble matter is leached by the hydrochloric acid, followed by solvent extraction and precipitation (the DHA method). In comparison, the total leaching rate of the rare earth elements was 94.6% by DHA, which is much higher than 42.08% achieved by the traditional method. The leaching rate of Y, Eu, Ce and Tb reached 94.6%, 99.05%, 71.45%, and 76.22%, respectively. DHA can decrease the consumption of chemicals and energy. The suggested DHA method is feasible for industrial applications

Effect of rare earth elements on uranium electrodeposition in LiCl-KCI eutectic salt

International Nuclear Information System (INIS)

Park, Sung Bin; Kang, Young Ho; Hwang, Sung Chan; Lee, Han Soo; Peak, Seung Woo; Ahn, Do Hee

2015-01-01

It is necessary to investigate the electrodeposition behavior of uranium and other elements on the cathode in the electrorefining process to recover the uranium selectively from the reduced metals of the electrolytic reduction process since transuranic elements and rare earth elements is dissolved in the LiCl-KCl eutectic salt. Study on separation factors of U, Ce, Y and Nd based on U and Ce was performed to investigate the deposition behavior of the cathode with respect to the concentration of rare earth elements in LiCl-KCl eutectic salt. After electrorefining with constant current mode by using Ce metal as a sacrifice anode, the contents of U, Ce, Y and Nd in the salt phase and the deposit phase of the cathode were analyzed, and separation factors of the elements were obtained from the analyses. Securing conditions of pure uranium recovery in the electrorefining process was investigated by considering the separation factors with respect to UCl 3 and CeCl 3 /UCl 3 ratio

Rare earth sulfates

International Nuclear Information System (INIS)

Komissarova, L.N.; Shatskij, V.M.; Pokrovskij, A.N.; Chizhov, S.M.; Bal'kina, T.I.; Suponitskij, Yu.L.

1986-01-01

Results of experimental works on the study of synthesis conditions, structure and physico-chemical properties of rare earth, scandium and yttrium sulfates, have been generalized. Phase diagrams of solubility and fusibility, thermodynamic and crystallochemical characteristics, thermal stability of hydrates and anhydrous sulfates of rare earths, including normal, double (with cations of alkali and alkaline-earth metals), ternary and anion-mixed sulfates of rare earths, as well as their adducts, are considered. The state of ions of rare earths, scandium and yttrium in aqueous sulfuric acid solutions is discussed. Data on the use of rare earth sulfates are given

Rare earth aerosol analysis by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Citron, I.M.; Mausner, L.F.

1982-01-01

An analytical method for the determination of four lanthanides in air filter samples is described. The method involves simultaneous quantitative determinations of La, Ce, Pr, and Nd at the microgram level by x-ray fluorescence spectrometry without chemical separation of these rare earths and without serious interferences from the dust matrices on the filters. The method has been used successfully to analyze some air filter samples collected at a rare earth processing refinery in Illinois. A description of the development of the method is given as well as the results obtained by using this method on the air filter samples. The reproducibility of the results was generally +-5%

Activation analysis of rare-earth elements in opium and cannabis samples. [Neutron reactions

Energy Technology Data Exchange (ETDEWEB)

Henke, G [Muenster Univ. (Germany, F.R.). Inst. fuer Pharmazeutische Chemie

1977-01-01

Rare-earth concentrations in 65 Opium, Cannabis and Cannabis resin samples seized from various parts of the world were determined by destructive NAA. Because of the greater concentrations of Ca, P, K, Fe, Na and Si in plant materials, rare-earth elements were isolated after neutron irradiation and determined by gamma-spectrometry. The main steps of the method are: Preashing of 1 g Cannabis resin, 2.5 g Cannabis, or 7.5 g Opium, respectively, in quartz ampoules (5 h, 500 deg C). Neutron irradiation, 24 h at 5x10/sup 13/n cm/sup -2/sec/sup -1/. Cooling period 2-3 days. After addition of 0.1 ..mu..Ci /sup 139/Ce and rare-earth carriers wet ashing of irradiated samples with H/sub 2/SO/sub 4//HNO/sub 3/, followed by alternate addition of HNO/sub 3/ and H/sub 2/O/sub 2/ (30%). Precipitation and removal of silicates, precipitation of fluorides, precipitation of hydroxides. Dissolution of hydroxides in HCl. Extraction with di-(2-ethylhexyl)phosphate (DEHP)/toluene and twice back-extraction of rare earths, gamma-spectrometry of HCl phase. Due to sample activity and half-life of nuclides, three measurements were made on each sample: 2 days (for La, Sm, Gd, Ho, Er, Yb); 14 days (for Nd, Lu) and 30 days after irradiation (for Ce, Eu, Tb). Great variations in absolute element concentrations, but only small significant differences of rare earth concentration ratios were found, indicating inconsiderable biogeochemical fractionation. The mean values of these ratios correspond to the relative abundances of the rare earths in the upper continental earth's crust.

Separation of pure Cerium oxides from rare earth compounds. Homogeneous precipitation using Urea-Hydrogen Peroxide

International Nuclear Information System (INIS)

Umeda, K.; Abrao, E.

1975-01-01

The obtainment of ceric oxide (CeO 2 ) of purity higher than 97% by application of homogeneous precipitation technique is described. The selective separation of cerium was reached by hydrolysis of urea in the presence of hydrogen peroxide, using a rare earths concentrate named rare earths chloride, a natural mixture of all lanthanides provenient from the industrialization of monazite. The best conditions for the preparation of CeO 2 of 94% purity are: 35-70g R 2 O 3 /1 and pH2,0 hydrolysis temperature: 88-90 0 C, urea/R 2 O 3 ratio: 4, H 2 O 2 /Ce 2 O 3 ratio: 1,5-5,0 and hydrolysis duration: 4 hours. A leaching procedure of the precipitate with 0,25-0,75M NHO 3 leads to a product of 97-99,5% CeO 2

Rare earth elements recycling from waste phosphor by dual hydrochloric acid dissolution

Energy Technology Data Exchange (ETDEWEB)

Liu, Hu [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Zhang, Shengen, E-mail: zhangshengen@mater.ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Pan, Dean; Tian, Jianjun; Yang, Min; Wu, Maolin [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Volinsky, Alex A. [Department of Mechanical Engineering, University of South Florida, Tampa, FL 33620 (United States)

2014-05-01

Highlights: • The article provides a new method for recycling rare earth (RE) from waste phosphor. • When compared with the traditional methods, leach rate was much higher. • Y–Eu concentrate and Tb–Ce concentrate were obtained successively. • It would reduce the burden of later extraction, separation and purification. - Abstract: This paper is a comparative study of recycling rare earth elements from waste phosphor, which focuses on the leaching rate and the technical principle. The traditional and dual dissolution by hydrochloric acid (DHA) methods were compared. The method of dual dissolution by hydrochloric acid has been developed. The Red rare earth phosphor (Y{sub 0.95}Eu{sub 0.05}){sub 2}O{sub 3} in waste phosphor is dissolved during the first step of acid leaching, while the Green phosphor (Ce{sub 0.67}Tb{sub 0.33}MgAl{sub 11}O{sub 19}) and the Blue phosphor (Ba{sub 0.9}Eu{sub 0.1}MgAl{sub 10}O{sub 17}) mixed with caustic soda are obtained by alkali sintering. The excess caustic soda and NaAlO{sub 2} are removed by washing. The insoluble matter is leached by the hydrochloric acid, followed by solvent extraction and precipitation (the DHA method). In comparison, the total leaching rate of the rare earth elements was 94.6% by DHA, which is much higher than 42.08% achieved by the traditional method. The leaching rate of Y, Eu, Ce and Tb reached 94.6%, 99.05%, 71.45%, and 76.22%, respectively. DHA can decrease the consumption of chemicals and energy. The suggested DHA method is feasible for industrial applications.

Influence of rare earths on shrinkage porosity in thin walled ductile cast iron

DEFF Research Database (Denmark)

Pedersen, Karl Martin; Tiedje, Niels Skat

2009-01-01

Ductile cast iron has been cast in test bars with thickness from 2 to 10 mm. The rare earth elements La and Ce have been added to some of the castings to evaluate their influence on microstructure and shrinkage tendency. Both La and Ce increased the graphite nodule count, especially for thickness...

The significant role of the rare earth ions on the elastic and thermodynamic parameters of LiCoDy- and ZnCoCe-ferrites

Energy Technology Data Exchange (ETDEWEB)

Bishay, Samiha T. [Physics Department, Faculty of Girls for Science, Art and Education Ain Shams University, Asma Fahmi Street, Heliopolis, Cairo (Egypt)]. E-mail: dr_samiha@hotmail.com

2006-06-15

Two types of rare earth ferrites [Li{sub 0.6}Co{sub 0.1}Dy{sub x}Fe{sub 2.3-x}O{sub 4}; 0.0=Ce{sub y}Fe{sub 2-y}O{sub 4}; 0.0=rare earth content as well as its ionic radius plays a significant role in the evaluated parameters. According to the experimental results, the two investigated types of rare earth ferrite are considered as insulator magnetic solids. It was found that for each composition there exists a characteristic temperature, down to which the resonance frequency of the investigated samples drops smoothly, but above this temperature the resonance frequency stays constant. Accordingly, these samples seem to be of importance in industrial applications especially in the field of electronics.

Study of the oxygen reduction reaction using Pt-Rare earths (La, Ce, Er) electrocatalysts for application of PEM fuel cells

International Nuclear Information System (INIS)

Gomes, Thiago Bueno

2013-01-01

The complexity of the oxygen reduction reaction (ORR) and its potential losses make it responsible for the most part of efficiency losses at the Fuel Cells. For this reaction the electrocatalyst witch is most appropriated and shows better performance is platinum, a noble metal that elevates the cost, raising barriers for Fuel Cells technology to enter the market. First this work focuses on reducing the amount of platinum used in the cathode, by being replaced by rare earths. The most common methods of synthesis involves a large amount of steps and this work proposed to prepare the electrocatalyst through a simpler way that would not take so many steps and time to be done. Using an ultrasound mixer the electrocatalyst was prepared mixing platinum supported on carbon black and the rare earths lanthanum, cerium and erbium oxides to be applied in a half-cell study of the ORR. The Koutecky-Levich plots shows that among the electrocatalysts prepared the Pt80Ce20/C had the catalytic activity close to the commercial BASF platinum on carbon black, suggesting that the reaction was taken by the 4-electron path. As found in some works in literature, among the rare earth used to study the ORR, cerium is the one witch shows the better performance because it is able to store and provide oxygen. This feature is of great interest for the ORR because this reaction is first order to the oxygen concentration. Results show that is possible to reduce the amount of platinum maintaining the same electrocatalyst activity. (author)

Mechanochemical decomposition of monazite to assist the extraction of rare earth elements

Energy Technology Data Exchange (ETDEWEB)

Kim, Wantae; Bae, Inkook; Chae, Soochun [Korea Institute of Geoscience and Mineral Resources, 92 Gwahang-no, Yuseong-gu, Daejeon 305-350 (Korea, Republic of); Shin, Heeyoung, E-mail: hyshin@kigam.re.k [Korea Institute of Geoscience and Mineral Resources, 92 Gwahang-no, Yuseong-gu, Daejeon 305-350 (Korea, Republic of)

2009-11-03

Mechanochemical decomposition by milling a mixture of monazite and sodium hydroxide powder and subsequent leaching by sulfuric acid for the extraction of rare earth elements at room temperature has been investigated. The milling of the mixture allows the mechanochemical formation of rare earth hydroxides and sodium phosphate as milling progresses. Nearly all the monazite is decomposed within 120 min under the present milling conditions. A 0.05N sulfuric acid solution enables us to improve the yield of each of La, Nd and Sm to around 85% or more in the powder milled for 120 min. Also, respective Ce and Pr yields of about 20% and 70% remain un-dissolved since they are changed into oxide forms during and after the milling operation. These rare earth oxides are mostly dissolved as the acid concentration increases to 5N. The yield of rare earth elements increases with increasing milling time. Thus mechanochemical milling plays a significant role in achieving high yield of rare earth elements from the leaching of the milled powder.

Mechanochemical decomposition of monazite to assist the extraction of rare earth elements

International Nuclear Information System (INIS)

Kim, Wantae; Bae, Inkook; Chae, Soochun; Shin, Heeyoung

2009-01-01

Mechanochemical decomposition by milling a mixture of monazite and sodium hydroxide powder and subsequent leaching by sulfuric acid for the extraction of rare earth elements at room temperature has been investigated. The milling of the mixture allows the mechanochemical formation of rare earth hydroxides and sodium phosphate as milling progresses. Nearly all the monazite is decomposed within 120 min under the present milling conditions. A 0.05N sulfuric acid solution enables us to improve the yield of each of La, Nd and Sm to around 85% or more in the powder milled for 120 min. Also, respective Ce and Pr yields of about 20% and 70% remain un-dissolved since they are changed into oxide forms during and after the milling operation. These rare earth oxides are mostly dissolved as the acid concentration increases to 5N. The yield of rare earth elements increases with increasing milling time. Thus mechanochemical milling plays a significant role in achieving high yield of rare earth elements from the leaching of the milled powder.

Rare earths

International Nuclear Information System (INIS)

1984-01-01

The conference was held from September 12 to 13, 1984 in Jetrichovice, Czechoslovakia. The participants heard 16 papers of which 4 were inputted in INIS. These papers dealt with industrial separation processes of rare earths, the use of chemical methods of separation from the concentrate of apatite and bastnesite, the effect of the relative permittivity of solvents in the elution of rare earth elements from a cation exchanger, and the determination of the content of different rare earth elements using X-ray fluorescence analysis and atomic absorption spectroscopy. (E.S.)

High coercivity rare earth-transition metal magnets

International Nuclear Information System (INIS)

Croat, J.J.

1982-01-01

Ferromagnetic compositions having intrinsic magnetic coercivities at room temperature of at least 1,000 Oersteds are formed by the controlled quenching of molten rare earth-transition metal alloys. Hard magnets may be inexpensively formed from the lower atomic weight lanthanide elements and iron. The preferable compositions lie within: at least one of Fe, Ni, Co; 20 - 70 atomic percent: at least one of Ce, Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, Tm, Y; 80 - 30 atomic percent. (author)

Towards atomic scale engineering of rare-earth-doped SiAlON ceramics through aberration-corrected scanning transmission electron microscopy

International Nuclear Information System (INIS)

Yurdakul, Hilmi; Idrobo, Juan C.; Pennycook, Stephen J.; Turan, Servet

2011-01-01

Direct visualization of rare earths in α- and β-SiAlON unit-cells is performed through Z-contrast imaging technique in an aberration-corrected scanning transmission electron microscope. The preferential occupation of Yb and Ce atoms in different interstitial locations of β-SiAlON lattice is demonstrated, yielding higher solubility for Yb than Ce. The triangular-like host sites in α-SiAlON unit cell accommodate more Ce atoms than hexagonal sites in β-SiAlON. We think that our results will be applicable as guidelines for many kinds of rare-earth-doped materials.

The environmental toxicology of rare earth elements (147Pm, 141Ce, 147Nd) and their safety evaluation in environment

International Nuclear Information System (INIS)

Chen Zuyi; Liu Yu; Cheng Wei; Zhang Ligan; Li Huixin; Wang Yuanxing

2001-01-01

The environmental behaviour, bioconcentration of rare earth elements and their effects on the animal gonadial hormone secretion were studied using the radioisotope tracer. The results were as follows: (1) The 147 Pm, 141 Ce and 147 Nd have strong adsorption in soil. They accumulated in soil easily and belonged to the matter which was difficult to move. When in water body, they concentrated in the bottom mud. (2) The authors tested bioconcentration factors (BCF) of 5 aquatics and absorption coefficients of 3 aquatic vegetables on 147 Pm, and their concentration in edible organ-stems. The materials for study showed apparent concentrating capabilities. (3) The distribution of 147 Pm, 141 Ce and 147 Nd residues were uneven in the animal's viscera and tissue. But, the higher residues were in bone, marrow, eye, brain, heart, adipose and testis, and their accumulation increased with dosage and time, which showed selective accumulation. There were much higher accumulation of RE in bone than in other viscera and tissues, and 141 Ce was highest in eye. (4) With the Nd or Ce of dose 200 mg/kg by once intraperitoneally, gonadial hormone (testosterone or progesterone) concentration in the serum decreased significantly compared with the control. This showed apparent inhibition on gonadial hormone secretion in mice; however with different dosages of Ce (200 and 800 mg/kg · d) in feed, the testosterone concentration of serum made no significant difference, but, the misshape rate of spermatozoon proved higher, and the misshape rate increased with feeding time and dosage. Rudimentary exploration on safety of agricultural use of Re for eco-environment are made, and some suggestions are proposed

Rare earth silicate (Ce, La, Nd, Ca, Th) SiO4 and cheralite (Th, Ca, Ce, La) (Psi)O4 are the responsible minerals for the anomalies of Morro de Ferro

International Nuclear Information System (INIS)

Fujimori, K.

1982-01-01

The Rare Earth silicate (La, Ce, Nd, Ca, Th)SiO 4 and cheralite (identified by Prof. Freeborn on a sample prepared from drilling core) were recognized as the most probable radioactive minerals that gave origin to high radioactive anomaly at Morro do Ferro hill together with coffinite, thorite, pyrochlore, apatite, etc., that are found in small quantity. The acids produced by decomposition of pyrite and fluorite have etched these radioactive minerals giving the high radioactive anomaly caracterized by high grade desiquilibrium of 232 Th serie. (Author) [pt

Rare earth ion controlled crystallization of mica glass-ceramics

International Nuclear Information System (INIS)

Garai, Mrinmoy; Karmakar, Basudeb

2016-01-01

In understanding the effects of rare earth ions to control the crystallization and microstructure of alkaline boroaluminosilicate system, the CeO_2, Nd_2O_3, Sm_2O_3 and Gd_2O_3 doped K_2O−MgO−B_2O_3−Al_2O_3−SiO_2−F glasses were synthesized by melt-quenching at 1550 °C. Higher density (2.82–3.06 g cm"−"3) and thermal stability (glass phase) is experiential on addition of rare earth content, which also affects in increasing the glass transition temperature (T_g) and crystallization temperature (T_c). Decrease of thermal expansion in glasses with rare earth ion content is maintained by the stabilization of glass matrix owing to their large cationic field strength. A significant change in the non-isothermal DSC thermogram observed at 750–1050 °C is attributed to fluorophlogopite crystallization. Opaque glass-ceramics were prepared from such glasses by single step heat-treatment at 1050 °C; and the predominant crystalline phases are identified as fluorophlogopite mica, KMg_3(AlSi_3O_1_0)F_2 by XRD and EDX analysis. The compact glass-ceramic microstructure by the agglomeration of fluorophlogopite mica crystallites (crystal size ∼ 100–500 nm, FESEM) is achieved in attendance of rare earth ion; and such microstructure controlled the variation of density, thermal expansion and microhardness value. Higher thermal expansion (11.11–14.08 × 10"−"6/K at 50–800 °C and 50–900 °C) of such glass-ceramics approve that these rare earth containing glasses can be useful for high temperature vacuum sealing application with metal or solid electrolyte. The increase of Vickers microhardness (5.27–5.61 GPa) in attendance of rare earth ions is attributed to the compact crystallinity of fluorophlogopite mica glass-ceramic microstructure. - Highlights: • Synthesis of rare earth oxide doped alkaline boroaluminosilicate glasses. • Development of opaque fluorophlogopite mica glass-ceramics by single-step heat treatment. • Nanocrystalline glass

High coercivity rare earth-transition metal magnets

International Nuclear Information System (INIS)

Croat, J.J.

1982-01-01

Ferromagnetic compositions having intrinsic magnetic coercivities at room temperature of at least 1,000 Oersteds are formed by the controlled quenching of molten rare earth -transition metal alloys. Hard magnets may be inexpensively formed from the lower atomic weight lanthanide elements and iron. The preferable compositions lie within: at least one of Fe, Ni, Co (20 to 70 atomic percent); and at least one of Ce, Pr, Na, Sm, Eu, Tb, Dy, Ho, Er, Tm, Y (80 to 30 atomic percent). (author)

Extraction of rare earths from iron-rich rare earth deposits

OpenAIRE

Bisaka, K.; Thobadi, I.C.; Pawlik, C.

2017-01-01

Rare earth metals are classified as critical metals by the United Nations, as they have found wide application in the fabrication of magnets, particularly those used in green energy technologies which mitigate global warming. Processing of ores containing rare earth elements is complex, and differs according to the nature of each ore. In the conventional process, run of mine (ROM) ores are processed in a physical separation plant to produce a concentrate from which rare earth elements are ext...

Processing of Pakistani carbonatites for separation of cerium from adjacent rare earths

International Nuclear Information System (INIS)

Akram, M.; Qazi, N.K.; Khan, M.F.; Hasan, G.H.; Ahmed, N.; Chughtai, N.A.

2003-01-01

% (v/v) for the ratio 1:4. The optimum extraction and stripping times being 30 minutes for each. The rare earths concentrate (i.e. REs salt) produced using the optimum parameters contained approx. 50% REO (w/w). For separation of cerium from adjacent rare earths, the rare earths concentrate was effectively dissolved in 10% HCl at 60 deg. C after 3hrs stirring. The chloride solution was oxidized with sodium hypochlorite at pH 3-4 to form precipitates of Ce(OH)/sub 4/ and Ln(OH)/sub 3/. These precipitates when filtered and leached with 3% HCl gave Ce(OH)/sub 4/ Cake containing -80% of cerium present in the concentrate. The cake contained mainly cerium with <5% other rare earths. The trivalent rare earths were soluble in HCl which separated as LnCl/sub 3/ in filtrate. Cerium was isolated in the form of ceric salt from the adjacent rare earths. (author)

Tetracyanidoborates with triply charged rare earth metal cations and their optical properties

International Nuclear Information System (INIS)

Hackbarth, Liisa

2015-01-01

The aim of this thesis is the description of the synthesis and characterization of a new group of tetracyanidoborates: tetracyanidoborates with trivalent rare earth metal cations. Their optical properties in the ultraviolet and visible range are also discussed. Common synthetic routes for tetracyanidoborates are adapted and applied to the preparation of the rare earth tetracyanidoborate hydrates. They are accessible with high yields and high purity through a reaction between the tetracyanidoboronic acid and rare earth hydroxides. It is shown that the rare earth tetracyanidoborates form isostructural groups, like the [LRE(H_2O)_5][B(CN)_4]_3.0.5 H_2O, where LRE"3"+ is La, Ce, Pr, Nd, Sm, Eu and Gd, the [HRE(H_2O)_7][B(CN)_4]_3 and the [HRE(H_2O)_8][B(CN)_4]_3.3 H_2O, where HRE"3"+ is Tb, Dy, Ho, Er, Tm, Yb, Lu and Y. Furthermore, the coordination number 9 is noticed to be common among the light rare earth cations, whereas the minor coordination number 8 is prevalent for the heavy rare earth cations in their tetracyanidoborates. This different construction of the coordination spheres between light and heavy rare earth cations leads to different structures depending on the energetic efficiency of the structural arrangement. Generally, the rare earth tetracyanidoborate hydrates are found to crystallize in the monoclinic crystal system. Moreover, other different crystal structures are observed depending on the crystallization temperature and the type of coordinated ligands and co-crystallized solvent molecules. The tetracyanidoborate hydrates with triply charged rare earth cations are characterized comprehensively by X-ray diffraction, vibrational spectroscopy, NMR-spectroscopy as well as by thermal analysis. Furthermore, the optical properties of some dehydrated rare earth tetracyanidoborates are investigated by UV-spectroscopy and luminescence measurements. The results of the optical measurements indicate that the tetracyanidoborates with rare earth metal cations

Magnetic interactions in equi-atomic rare-earth intermetallic alloys RScGe (R = Ce, Pr, Nd and Gd) studied by time differential perturbed angular correlation spectroscopy and ab initio calculations.

Science.gov (United States)

Mishra, S N

2009-03-18

Applying the time differential perturbed angular correlation (TDPAC) technique we have measured electric and magnetic hyperfine fields of the (111)Cd impurity in equi-atomic rare-earth intermetallic alloys RScGe (R = Ce, Pr and Gd) showing antiferro- and ferromagnetism with unusually high ordering temperatures. The Cd nuclei occupying the Sc site show high magnetic hyperfine fields with saturation values B(hf)(0) = 21 kG, 45 kG and 189 kG in CeScGe, PrScGe and GdScGe, respectively. By comparing the results with the hyperfine field data of Cd in rare-earth metals and estimations from the RKKY model, we find evidence for the presence of additional spin density at the probe nucleus, possibly due to spin polarization of Sc d band electrons. The principal electric field gradient component V(zz) in CeScGe, PrScGe and GdScGe has been determined to be 5.3 × 10(21) V m(-2), 5.5 × 10(21) V m(-2) and 5.6 × 10(21) V m(-2), respectively. Supplementing the experimental measurements, we have carried out ab initio calculations for pure and Cd-doped RScGe compounds with R = Ce, Pr, Nd and Gd using the full potential linearized augmented plane wave (FLAPW) method based on density functional theory (DFT). From the total energies calculated with and without spin polarization we find ferrimagnetic ground states for CeScGe and PrScGe while NdScGe and GdScGe are ferromagnetic. In addition, we find a sizable magnetic moment at the Sc site, increasing from ≈0.10 μ(B) in CeScGe to ≈0.3 μ(B) in GdScGe, confirming the spin polarization of Sc d band electrons. The calculated electric field gradient and magnetic hyperfine fields of the Cd impurity closely agree with the experimental values. We believe spin polarization of Sc 3d band electrons, strongly hybridized with spin polarized 5d band electrons of the rare-earth, enables a long range Ruderman-Kittel-Kasuya-Yosida (RKKY) interaction between RE 4f moments which in turn leads to high magnetic ordering temperatures in

China's rare-earth industry

Science.gov (United States)

Tse, Pui-Kwan

2011-01-01

Introduction China's dominant position as the producer of over 95 percent of the world output of rare-earth minerals and rapid increases in the consumption of rare earths owing to the emergence of new clean-energy and defense-related technologies, combined with China's decisions to restrict exports of rare earths, have resulted in heightened concerns about the future availability of rare earths. As a result, industrial countries such as Japan, the United States, and countries of the European Union face tighter supplies and higher prices for rare earths. This paper briefly reviews China's rare-earth production, consumption, and reserves and the important policies and regulations regarding the production and trade of rare earths, including recently announced export quotas. The 15 lanthanide elements-lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium (atomic numbers 57-71)-were originally known as the rare earths from their occurrence in oxides mixtures. Recently, some researchers have included two other elements-scandium and yttrium-in their discussion of rare earths. Yttrium (atomic number 39), which lies above lanthanum in transition group III of the periodic table and has a similar 3+ ion with a noble gas core, has both atomic and ionic radii similar in size to those of terbium and dysprosium and is generally found in nature with lanthanides. Scandium (atomic number 21) has a smaller ionic radius than yttrium and the lanthanides, and its chemical behavior is intermediate between that of aluminum and the lanthanides. It is found in nature with the lanthanides and yttrium. Rare earths are used widely in high-technology and clean-energy products because they impart special properties of magnetism, luminescence, and strength. Rare earths are also used in weapon systems to obtain the same properties.

THE EFFECTS OF RARE EARTHS ON ACTIVITY AND SURFACE ...

African Journals Online (AJOL)

A series of Ru-RE/γ-AL2O3 (RE = Ce, Pr, La, Sm, Tb or Gd) and Ru/γ-AL2O3 catalysts were prepared by impregnation method. The influence of rare earths on the catalytic performance of Ru/γ-AL2O3 catalyst for the water gas shift reaction was studied. The catalysts were characterized by X-ray diffraction (XRD), ...

Synthesis and investigation of some physicochemical properties of rare earth nitrobarbiturates

International Nuclear Information System (INIS)

Biryulina, V.N.; Chupakhina, R.A.; Serebrennikov, V.V.

1984-01-01

Crystal depositions of L 3 MnH 2 O composition where L is anion of nitrobarbituric acid C 4 H 2 N 3 O 5 - ; M is rare earth ion excluding Ce 3+ and Pm 3+ ; n=12 are extracted under dissolution of freshly prepared hydroxides of rare earth elements (REE) in ethanol aqueous solution of nitrobarbituric acid. The method of IR spectroscopy has been applied to disclose relation of rare earth ion with groups of C=0 acid. The method of derivatography has been used to study thermolysis of REE nitrobarbiturates; dehydration proceeds in two stages with decrease of temperature of the beginning of dehydration by 20 deg C in the La 3+ → Lu 3+ series. The curve of dependence of REE nitrobarbiturate solubility in water at 25 deg C on serial number of REE passes through the minimum accounted for Sm 3+

Crystal fields at light rare-earth ions in Y and Lu

DEFF Research Database (Denmark)

Touborg, P.; Nevald, Rolf; Johansson, Torben

1978-01-01

Crystal-field parameters have been deduced for the light rare-earth solutes Ce, Pr, and Nd in Y or Lu hosts from measurements of the paramagnetic susceptibilities. In the analysis all multiplets in the lowest LS term were included. For a given host, crystal-field parameters divided by Stevens fac...

Rare earth activated yttrium aluminate phosphors with modulated luminescence.

Science.gov (United States)

Muresan, L E; Popovici, E J; Perhaita, I; Indrea, E; Oro, J; Casan Pastor, N

2016-06-01

Yttrium aluminate (Y3 A5 O12 ) was doped with different rare earth ions (i.e. Gd(3+) , Ce(3+) , Eu(3+) and/or Tb(3+) ) in order to obtain phosphors (YAG:RE) with general formula,Y3-x-a Gdx REa Al5 O12 (x = 0; 1.485; 2.97 and a = 0.03). The synthesis of the phosphor samples was done using the simultaneous addition of reagents technique. This study reveals new aspects regarding the influence of different activator ions on the morpho-structural and luminescent characteristics of garnet type phosphor. All YAG:RE phosphors are well crystallized powders containing a cubic-Y3 Al5 O12 phase as major component along with monoclinic-Y4 Al2 O9 and orthorhombic-YAlO3 phases as the impurity. The crystallites dimensions of YAG:RE phosphors vary between 38 nm and 88 nm, while the unit cell slowly increase as the ionic radius of the activator increases. Under UV excitation, YAG:Ce exhibits yellow emission due to electron transition in Ce(3+) from the 5d level to the ground state levels ((2) F5/2 , (2) F7/2 ). The emission intensity of Ce(3+) is enhanced in the presence of the Tb(3+) ions and is decreased in the presence of Eu(3+) ions due to some radiative or non-radiative processes that take place between activator ions. By varying the rare earth ions, the emission colour can be modulated from green to white and red. Copyright © 2015 John Wiley & Sons, Ltd. Copyright © 2015 John Wiley & Sons, Ltd.

Photo-Induced conductivity of heterojunction GaAs/Rare-Earth doped SnO2

Directory of Open Access Journals (Sweden)

Cristina de Freitas Bueno

2013-01-01

Full Text Available Rare-earth doped (Eu3+ or Ce3+ thin layers of tin dioxide (SnO2 are deposited by the sol-gel-dip-coating technique, along with gallium arsenide (GaAs films, deposited by the resistive evaporation technique. The as-built heterojunction has potential application in optoelectronic devices, because it may combine the emission from the rare-earth-doped transparent oxide, with a high mobility semiconductor. Trivalent rare-earth-doped SnO2 presents very efficient emission in a wide wavelength range, including red (in the case of Eu3+ or blue (Ce3+. The advantage of this structure is the possibility of separation of the rare-earth emission centers, from the electron scattering, leading to an indicated combination for electroluminescence. Electrical characterization of the heterojunction SnO2:Eu/GaAs shows a significant conductivity increase when compared to the conductivity of the individual films. Monochromatic light excitation shows up the role of the most external layer, which may act as a shield (top GaAs, or an ultraviolet light absorber sink (top RE-doped SnO2. The observed improvement on the electrical transport properties is probably related to the formation of short conduction channels in the semiconductors junction with two-dimensional electron gas (2DEG behavior, which are evaluated by excitation with distinct monochromatic light sources, where the samples are deposited by varying the order of layer deposition.

A reactive distillation process for the treatment of LiCl-KCl eutectic waste salt containing rare earth chlorides

Energy Technology Data Exchange (ETDEWEB)

Eun, H.C., E-mail: ehc2004@kaeri.re.kr; Choi, J.H.; Kim, N.Y.; Lee, T.K.; Han, S.Y.; Lee, K.R.; Park, H.S.; Ahn, D.H.

2016-11-15

The pyrochemical process, which recovers useful resources (U/TRU metals) from used nuclear fuel using an electrochemical method, generates LiCl-KCl eutectic waste salt containing radioactive rare earth chlorides (RECl{sub 3}). It is necessary to develop a simple process for the treatment of LiCl-KCl eutectic waste salt in a hot-cell facility. For this reason, a reactive distillation process using a chemical agent was achieved as a method to separate rare earths from the LiCl-KCl waste salt. Before conducting the reactive distillation, thermodynamic equilibrium behaviors of the reactions between rare earth (Nd, La, Ce, Pr) chlorides and the chemical agent (K{sub 2}CO{sub 3}) were predicted using software. The addition of the chemical agent was determined to separate the rare earth chlorides into an oxide form using these equilibrium results. In the reactive distillation test, the rare earth chlorides in LiCl-KCl eutectic salt were decontaminated at a decontamination factor (DF) of more than 5000, and were mainly converted into oxide (Nd{sub 2}O{sub 3}, CeO{sub 2}, La{sub 2}O{sub 3}, Pr{sub 2}O{sub 3}) or oxychloride (LaOCl, PrOCl) forms. The LiCl-KCl was purified into a form with a very low concentration (<1 ppm) for the rare earth chlorides.

Rare earth conversion coatings grown on AA6061 aluminum alloys. Corrosion studies

Energy Technology Data Exchange (ETDEWEB)

Brachetti S, S. B. [Instituto Tecnologico de Ciudad Madero, Av. 1o. de Mayo y Sor Juana I. de la Cruz, Col. Los Mangos, 89440 Ciudad Madero, Tanaulipas (Mexico); Dominguez C, M. A.; Torres H, A. M.; Onofre B, E. [IPN, Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada - Altamira, Carretera Tampico-Puerto Industrial Altamira Km. 14.5, 89600 Altamira, Tamaulipas (Mexico); De la Cruz H, W., E-mail: mdominguezc@ipn.mx [UNAM, Centro de Nanociencias y Nanotecnologia, Apdo. Postal 2681, 22800 Ensenada, Baja California (Mexico)

2014-07-01

The present work is aimed to investigate the corrosion resistance of rare earth protective coatings deposited by spontaneous deposition on AA6061 aluminum alloy substrates. Coatings were deposited from water-based Ce(NO{sub 3}){sub 3} and La(NO{sub 3}){sub 3} solutions by varing parameters such as rare earth solution concentration, bath temperature and immersion time. The values of the Tafel slopes indicate that the cathodic process is favored by concentration polarization rather than activation polarization. Chemical and morphological characterizations of the surface before and after electrochemical evaluations were performed by X-ray photoelectron spectroscopy and scanning electron microscopy. (Author)

Rare earth conversion coatings grown on AA6061 aluminum alloys. Corrosion studies

International Nuclear Information System (INIS)

Brachetti S, S. B.; Dominguez C, M. A.; Torres H, A. M.; Onofre B, E.; De la Cruz H, W.

2014-01-01

The present work is aimed to investigate the corrosion resistance of rare earth protective coatings deposited by spontaneous deposition on AA6061 aluminum alloy substrates. Coatings were deposited from water-based Ce(NO 3 ) 3 and La(NO 3 ) 3 solutions by varing parameters such as rare earth solution concentration, bath temperature and immersion time. The values of the Tafel slopes indicate that the cathodic process is favored by concentration polarization rather than activation polarization. Chemical and morphological characterizations of the surface before and after electrochemical evaluations were performed by X-ray photoelectron spectroscopy and scanning electron microscopy. (Author)

Synthesis and physicochemical investigation of 3-nitro-5-aminobenzoates of rare earths

International Nuclear Information System (INIS)

Makushova, G.N.; Zakharova, T.V.; Shilova, L.I.

1994-01-01

The compounds of cerium subgroup rare earth with 3-nitro-5-aminobenzoic acid of composition Ln(C 7 H 5 N 2 O 4 ) 3 ·nH 2 O, where Ln-La, Ce, Pr, Nd, Sm, Eu; n=4-14 not yet described in literature were obtained. Rare earth 3-nitro-5-aminobenzoates were individual crystal substances, as shown by X-ray diffraction; their interplanar distances were calculated. Thermal stability of the derived compounds was studied by means of thermography and thermal gravimetry. The interval of dehydration and start of decomposition of anhydrous salts was determined

Rare earth impurities in high purity lanthanum oxide determined by neutron activation analysis

International Nuclear Information System (INIS)

Nguyen Van Suc; Desai, H.B.; Parthasarathy, R.; Gangadharan, S.

1992-01-01

Individual rare earth impurities in high purity La 2 O 3 (≥99.9%) have been determined by NAA after pre-separation of the matrix (La). The separation is carried out on an anion exchanger (Dowex 1x8) using different mixtures of methanol/nitric acid as eluants. The rare earth elements from Dy to Lu are eluted quantitatively using a 10% 1M HNO 3 - 90% methanol mixture, while the light rare earths from Ce to Gd are eluted quantitatively using a 10% 0.05M HNO 3 - 90% methanol mixture. La, which is retained on the column, is eluted using 0.1M HNO 3 . The recoveries of the various rare earth elements have been checked using radiotracers and also by spiking the sample with known amount of elements, and the recoveries are found to be quantitative. Results obtained on a typical high purity lanthanum oxide are reported here. (author) 5 refs.; 1 fig

The Marine Geochemistry of the Rare Earth Elements

Science.gov (United States)

1983-09-01

C3): 2045-2056. BACON, M.P., P.G. BREWER, D.W. SPENCER, T.W. MURRAY & T. GODDARD (1980). Lead - 210 , polonium - 210 , manganese and iron in the Cariaco...191 La and Pr 197 Ce: its oxidation and reduction 197 Eu 207 4.5. Conclusions 210 CHAPTER 5. Behaviour of the Rare Earth Elements in anoxic waters of...seawater and algal food . When the radioactive particles were no longer available, the accumulated radioactivity of the zooplankters was rapidly lost

Effects of rare earth metals addition on the resistance to pitting corrosion of super duplex stainless steel - Part 1

International Nuclear Information System (INIS)

Kim, Soon-Tae; Jeon, Soon-Hyeok; Lee, In-Sung; Park, Yong-Soo

2010-01-01

To elucidate the effects of rare earth metals addition on the resistance to pitting corrosion of super duplex stainless steel, a metallographic examination, potentiodynamic and potentiostatic polarization tests, a SEM-EDS and a SAM analysis of inclusion, austenite phase and ferrite phase were conducted. The addition of rare earth metals to the base alloy led to the formation of (Mn, Cr, Si, Al, Ce) oxides and (Mn, Cr, Si, Ce) oxides, which improved the resistance to pitting corrosion and caused a decrease in the preferential interface areas for the initiation of the pitting corrosion.

Rare earth octacyanomolybdates(4)

International Nuclear Information System (INIS)

Zubritskaya, D.I.; Sergeeva, A.N.; Pisak, Yu.V.

1980-01-01

Optimal conditions for synthesis of rare-earth octacyanomolybdates(4) of the Ln 4 [Mo(CN) 8 ] 3 xnH 2 O composition (where Ln is a rare-earth element, other than Pr, Pm, Lu, Tb) have been worked out. The synthesis has been accomplished by neutralization with octacianomolybdic acid with rare-earth carbonates. The composition and structure of the compounds synthesized have been studied by infrared-spectroscopy. It has been established that rare-earth octacyanomolybdates(4) form three isostructural groups

Synthesis and sorption properties of new synthesized rare-earth-doped sodium titanate

International Nuclear Information System (INIS)

Ali, I.M.

2010-01-01

A series of rare-earth-doped sodium titanates with the chemical formula R x H y Na 4-(x+y) TiO 4 ·nH 2 O (where R = Ce 3+ , Nd 3+ and Sm 3+ ) were grown employing solid-state fusion reaction technique. The physico-chemical investigations indicated that the new materials were self engineered into large particles enough to be used in sorption process and having crystalline structures containing localized Na + ions. Equilibrium studies revealed that an enhancement in sorption efficiency of sodium titanate after rare-earth doping. The neodymium-rich sodium titanate exhibited a better exchange affinity for Cs + compared to the other studied series. Data on the kinetics of cesium exchange fit well to pseudo-second order and intra-particle diffusion models. In a separate experiment, it was reported that the R-HNaTi series showed responsible sorption affinity toward Ce, Nd and Sm ions in their solution mixture with insignificant selectivity trend which reflects the high stability of titanate matrices. (author)

Low-temperature SCR of NO with NH{sub 3} over activated semi-coke composite-supported rare earth oxides

Energy Technology Data Exchange (ETDEWEB)

Wang, Jinping; Yan, Zheng; Liu, Lili; Zhang, Yingyi; Zhang, Zuotai; Wang, Xidong, E-mail: xidong@pku.edu.cn

2014-08-01

The catalysts with different rare earth oxides (La, Ce, Pr and Nd) loaded onto activated semi-coke (ASC) via hydrothermal method are prepared for the selective catalytic reduction (SCR) of NO with NH{sub 3} at low temperature (150–300 °C). It is evidenced that CeO{sub 2} loaded catalysts present the best performance, and the optimum loading amount of CeO{sub 2} is about 10 wt%. Composite catalysts by doping La, Pr and Nd into CeO{sub 2} are prepared to obtain further improved catalytic properties. The SCR mechanism is investigated through various characterizations, including XRD, Raman, XPS and FT-IR, the results of which indicate that the oxygen defect plays an important role in SCR process and the doped rare earth elements effectively serve as promoters to increase the concentration of oxygen vacancies. It is also found that the oxygen vacancies in high concentration are favored for the adsorption of O{sub 2} and further oxidation of NO, which facilitates a rapid progressing of the following reduction reactions. The SCR process of NO with NH{sub 3} at low temperature over the catalysts of ASC composite-supported rare earth oxides mainly follows the Langmuir–Hinshlwood mechanism.

Rare earth ion controlled crystallization of mica glass-ceramics

Energy Technology Data Exchange (ETDEWEB)

Garai, Mrinmoy; Karmakar, Basudeb, E-mail: basudebk@cgcri.res.in

2016-09-05

In understanding the effects of rare earth ions to control the crystallization and microstructure of alkaline boroaluminosilicate system, the CeO{sub 2}, Nd{sub 2}O{sub 3}, Sm{sub 2}O{sub 3} and Gd{sub 2}O{sub 3} doped K{sub 2}O−MgO−B{sub 2}O{sub 3}−Al{sub 2}O{sub 3}−SiO{sub 2}−F glasses were synthesized by melt-quenching at 1550 °C. Higher density (2.82–3.06 g cm{sup −3}) and thermal stability (glass phase) is experiential on addition of rare earth content, which also affects in increasing the glass transition temperature (T{sub g}) and crystallization temperature (T{sub c}). Decrease of thermal expansion in glasses with rare earth ion content is maintained by the stabilization of glass matrix owing to their large cationic field strength. A significant change in the non-isothermal DSC thermogram observed at 750–1050 °C is attributed to fluorophlogopite crystallization. Opaque glass-ceramics were prepared from such glasses by single step heat-treatment at 1050 °C; and the predominant crystalline phases are identified as fluorophlogopite mica, KMg{sub 3}(AlSi{sub 3}O{sub 10})F{sub 2} by XRD and EDX analysis. The compact glass-ceramic microstructure by the agglomeration of fluorophlogopite mica crystallites (crystal size ∼ 100–500 nm, FESEM) is achieved in attendance of rare earth ion; and such microstructure controlled the variation of density, thermal expansion and microhardness value. Higher thermal expansion (11.11–14.08 × 10{sup −6}/K at 50–800 °C and 50–900 °C) of such glass-ceramics approve that these rare earth containing glasses can be useful for high temperature vacuum sealing application with metal or solid electrolyte. The increase of Vickers microhardness (5.27–5.61 GPa) in attendance of rare earth ions is attributed to the compact crystallinity of fluorophlogopite mica glass-ceramic microstructure. - Highlights: • Synthesis of rare earth oxide doped alkaline boroaluminosilicate glasses. • Development of opaque

The occurrence of rare earth elements in some Finnish mires

Directory of Open Access Journals (Sweden)

Yliruokanen, I.

1995-12-01

Full Text Available The content of the more abundant rare earths (RE (Y, La, Ce, Pr, Nd and Sm in the ash of 399 peat samples from 26 Finnish mires was determined by X-ray fluorescence spectrometry. The content of all rare earths (La-Lu, Y in 29 samples was also determined by spark source mass spectrometry. The median RE contents in peat ashes from areas where the bedrock consists of rapakivi granite, granite or archean gneiss are reported. Detailed data concerning the individual mires are also presented. The highest RE contents were found in samples from rapakivi granite areas where a strong negative Eu anomaly was also observed. The RE contents were in general highest at the basal peat layers.

Rare earths and rare earth alloys electrolytic preparation process and device for this process

International Nuclear Information System (INIS)

Seon, F.; Barthole, G.

1986-01-01

Electrolysis of a molten salt of rare earth or rare earth alloy for preparation of the metal or alloy is described. The molten salt bath comprises at least a rare earth chloride, at least an alkaline or alkaline earth chloride and at least an alkaline or alkaline earth fluoride [fr

Tetracyanidoborates with triply charged rare earth metal cations and their optical properties

Energy Technology Data Exchange (ETDEWEB)

Hackbarth, Liisa

2015-11-24

The aim of this thesis is the description of the synthesis and characterization of a new group of tetracyanidoborates: tetracyanidoborates with trivalent rare earth metal cations. Their optical properties in the ultraviolet and visible range are also discussed. Common synthetic routes for tetracyanidoborates are adapted and applied to the preparation of the rare earth tetracyanidoborate hydrates. They are accessible with high yields and high purity through a reaction between the tetracyanidoboronic acid and rare earth hydroxides. It is shown that the rare earth tetracyanidoborates form isostructural groups, like the [LRE(H{sub 2}O){sub 5}][B(CN){sub 4}]{sub 3}.0.5 H{sub 2}O, where LRE{sup 3+} is La, Ce, Pr, Nd, Sm, Eu and Gd, the [HRE(H{sub 2}O){sub 7}][B(CN){sub 4}]{sub 3} and the [HRE(H{sub 2}O){sub 8}][B(CN){sub 4}]{sub 3}.3 H{sub 2}O, where HRE{sup 3+} is Tb, Dy, Ho, Er, Tm, Yb, Lu and Y. Furthermore, the coordination number 9 is noticed to be common among the light rare earth cations, whereas the minor coordination number 8 is prevalent for the heavy rare earth cations in their tetracyanidoborates. This different construction of the coordination spheres between light and heavy rare earth cations leads to different structures depending on the energetic efficiency of the structural arrangement. Generally, the rare earth tetracyanidoborate hydrates are found to crystallize in the monoclinic crystal system. Moreover, other different crystal structures are observed depending on the crystallization temperature and the type of coordinated ligands and co-crystallized solvent molecules. The tetracyanidoborate hydrates with triply charged rare earth cations are characterized comprehensively by X-ray diffraction, vibrational spectroscopy, NMR-spectroscopy as well as by thermal analysis. Furthermore, the optical properties of some dehydrated rare earth tetracyanidoborates are investigated by UV-spectroscopy and luminescence measurements. The results of the optical

Rare earths as a future resource

International Nuclear Information System (INIS)

Cornell, D.H.

1988-01-01

The fourteen rare earth or lanthanide elements have recently emerged as an important natural resource because of the rapidly growing demand in the electronic, chemical and metallurgical industries. The Symposium on rare earth elements as a future resource presented a multidisciplinary review of rare earth chemistry, geology, beneficiation, industrial applications and marketing. Papers by experts in many fields were presented on the following topics: chemical properties of the rare earth elements; the analysis of rare earth elements and minerals; beneficiation and extraction of rare earth elements; economic geochemistry and mineralogy of rare earths; present industrial uses of rare earth elements; the role of rare earth elements in high-temperature superconductors; the technical application of high-temperature superconductors; supply and demand for rare earth products - now and in the future, and the geology of rare earth deposits

Fiber-optic thermometer application of thermal radiation from rare-earth end-doped SiO2 fiber

International Nuclear Information System (INIS)

Katsumata, Toru; Morita, Kentaro; Komuro, Shuji; Aizawa, Hiroaki

2014-01-01

Visible light thermal radiation from SiO 2 glass doped with Y, La, Ce, Pr, Nd, Eu, Tb, Dy, Ho, Er, Tm, Yb, and Lu were studied for the fiber-optic thermometer application based on the temperature dependence of thermal radiation. Thermal radiations according to Planck's law of radiation are observed from the SiO 2 fibers doped with Y, La, Ce, Pr, Eu, Tb, and Lu at the temperature above 1100 K. Thermal radiations due to f-f transitions of rare-earth ions are observed from the SiO 2 fibers doped with Nd, Dy, Ho, Er, Tm, and Yb at the temperature above 900 K. Peak intensities of thermal radiations from rare-earth doped SiO 2 fibers increase sensitively with temperature. Thermal activation energies of thermal radiations by f-f transitions seen in Nd, Dy, Ho, Er, Tm, and Yb doped SiO 2 fibers are smaller than those from SiO 2 fibers doped with Y, La, Ce, Pr, Eu, Tb, and Lu. Thermal radiation due to highly efficient f-f transitions in Nd, Dy, Ho, Er, Tm, and Yb ions emits more easily than usual thermal radiation process. Thermal radiations from rare-earth doped SiO 2 are potentially applicable for the fiber-optic thermometry above 900 K

Resonance electronic Raman scattering in rare earth crystals

International Nuclear Information System (INIS)

Williams, G.M.

1988-01-01

The intensities of Raman scattering transitions between electronic energy levels of trivalent rare earth ions doped into transparent crystals were measured and compared to theory. A particle emphasis was placed on the examination of the effect of intermediate state resonances on the Raman scattering intensities. Two specific systems were studied: Ce 3+ (4f 1 ) in single crystals of LuPO 4 and Er 3+ (4f 11 ) in single crystals of ErPO 4 . 134 refs., 92 figs., 33 tabs

SEPARATION OF TRANSURANIC ELEMENTS FROM RARE EARTH COMPOUNDS

Science.gov (United States)

Kohman, T.P.

1961-11-21

A process of separating neptunium and plutonium values from rare earths and alkaline earth fission products present on a solid mixed actinide carrier (Th or U(IV) oxalate or fluoride) --fission product carrier (LaF/sub 3/, CeF/sub 3/, SrF/sub 2/, CaF/sub 2/, YF/sub 3/, La oxalate, cerous oxalate, Sr oxalate, Ca oxalate or Y oxalate) by extraction of the actinides at elevated temperature with a solution of ammonium fluoride and/or ammonium oxalate is described. Separation of the fission-product-containing carriers from the actinide solution formed and precipitation of the neptunium and plutonium from the solution with mineral acid are also accomplished. (AEC)

The electronic structure of rare-earth luminescent centre in alkaline-earth sulphides

International Nuclear Information System (INIS)

Zheng Qingqi; Pan Wei; Huang Maichun; He Xiaoguang

1988-09-01

The cluster method is used to investigate the electronic structure of rare-earth Eu 2+ and Ce 3+ doped SrS and CaS alkaline-earth sulphides in the local density theory regime. The ground state is obtained self-consistently by the DV-X α method, while the transition state theory is used to calculate the excited states. The energy difference between ground state and excited state is 2.95 eV (420 nm) for CaS:Eu is in good agreement with the experimental data of 430 nm for the absorption peak in SrS:Cu. The composition of ground state and excited state is also calculated which can give information about the EL excitation mechanism. (author). 7 refs, 4 figs, 3 tabs

Separation method for rare-earths using high-voltage electrophoresis on paper strip

International Nuclear Information System (INIS)

Clarence, J.

1966-01-01

The equipment includes an electrophoresis set running at 3 000 V and 20 mA. Two cooling plates are used as heat exchanger, and a pneumatic pressure device to insure an uniform pressure on the paper strip laid flat. The mobilities and the separations of the rare earths in lactic, and, α hydroxy-isobutyric acid solutions are investigated on cellulose acetate strip. Better results are obtained with α hydroxy-isobutyric acid. The method is rapid and allows a fine fractionation of rare earth elements within less than an hour. A complete separation of a Ce - Pr - Nd - Pm - Eu mixture, and a Y - Tb mixture is obtained. (author) [fr

Rare earth elements in the Pacific and Atlantic Oceans. [Pr, Tb, Ho, Tm, Lu, La, Nd, Sm, Eu, Gd, Yb, Ce

Energy Technology Data Exchange (ETDEWEB)

Baar, H J.W. de; Bacon, M P; Brewer, P G; Bruland, K W

1985-09-01

The first profiles of Pr, Tb, Ho, Tm and Lu in the Pacific Ocean, as well as profiles of La, Ce, Nd, Sm, Eu, Gd and Yb are reported. Concentrations of REE (except Ce) in the deep water are two to three times higher than those observed in the deep Atlantic Ocean. Surface water concentrations are typically lower than in the Atlantic Ocean, especially for the heavier elements Ho,Tm,Yb and Lu. Cerium is strongly depleted in the Pacific water column, but less so in the oxygen minimum zone. The distribution of the REE group is consistent with two simultaneous processes: (1) cycling similar to that of opal and calcium carbonate, and (2) adsorptive scavenging by settling particles and possibly by uptake at ocean boundaries. However, the first process can probably not be sustained by the low REE contents of shells, unless additional adsorption on surfaces is invoked. The second process, adsorptive scavenging, largely controls the oceanic distribution and typical seawater pattern of the rare earths. (author).

Radiochemical studies in chemical separation and spectrographic determination of rare earths in thorium oxide matrix (Preprint No. RA.06)

International Nuclear Information System (INIS)

Adya, V.C.; Dhawale, B.A.; Rajeshwari, B.; Bangia, T.R.; Sastry, M.D.

1989-01-01

A chemical separation procedure was standardised for the separation of traces of rare earths from ThO 2 matrix using HDEHP (Di 2-ethyl hexyl phosphoric acid). The studies were carried out using both nitric acid and hydrochloric acid medium in different concentrations. The extraction studies were also carried out using radioactive isotopes of rare earths viz. 141 Ce, 152-154 Eu, 153 Gd, 170 Tm etc. The extraction was effective in both media. In 0.1 M HDEHP/xylene and 3 M HNO 3 , Ce was partially extracted into organic phase. So HCl/xylene medium was chosen for extraction purposes. The recovery was confirmed by both gamma counting and emission spectropgraphic method. It was found to be quantitative within experimental error. The separation procedure development here was used for determination of rare earths in thorium oxide matrix by emission spectrographic method. (author)

Procedure for the separation of cerium from crude phosphates and rare earth concentrates

International Nuclear Information System (INIS)

Richter, H.; Koenig, O.; Schmitt, A.; Grauss, H.; Freitag, S.

1986-01-01

The invention has to do with a procedure for the separation of cerium from crude phosphates and rare earth phosphate concentrates originating from the partial neutralization of nitric crude phosphate decomposition solutions. It is aimed at the cerium separation from the raw material at an early stage of reprocessing without preceding elimination of other components and impurities. The rare earth phosphate concentrates or crude phosphates are dissolved in nitric acid, the Ce 3+ is oxidized with potassium permanganate or magnanese(IV) hydroxide, and cerium(IV) phosphate is precipitated as pure substance by decreasing the acidity of the solution

Rare earths 1998 market update

International Nuclear Information System (INIS)

Tourre, J.M.

1998-01-01

The rare earth industry has always been a world of rapid change with the emergence of new markets, new ores and new players, as well as the disappearance of old applications. Rare earth based products are used in a great diversity of applications such as hard disk drives, CD drives, batteries, capacitors, pigments, ceramics, polishing powders, fuel cells, flints, catalyst converter, fluid cracking catalysts, etc. South East Asia holds the largest share of the known reserve of rare earth ores and is one of the major markets for rare earth compounds; in the last ten years, China has become the largest producer of rare earth intermediates as well as an important exporter of separated rare earth elements. Today, China has approximately 150 factories producing rare earth compounds, most of which are experiencing financial difficulties due to the lack of knowledge of true market needs, lack of control of their distribution channels and production over-capacity. Recently the Chinese rare earth producers have recognized the situation and efforts are underway to rationalize rare earth production. Japan has dominated many of the major application markets, and is by far the largest market for metal and alloy products. This will remain the case for the next five years; however, new countries are emerging as significant users of rare earth products such as Korea, Taiwan and Malaysia. During the last ten years rare earth producers adjusted to several radical changes that affected the raw materials, the application mix and the price structure. New producers have emerged, especially from China; some have subsequently stopped their activities while others have focused their efforts in a specific market segment

Rare earths: occurrence, production and applications

International Nuclear Information System (INIS)

Murthy, T.K.S.; Mukherjee, T.K.

2002-01-01

The mining and processing of rare earth minerals, particularly of monazite, began in a modest way in 1880s for commercialized production of mantle for gas lighting. For all major applications up to mid-twentieth century- production of lighter flints, misch metal as a metallurgical alloying agent, colouring, decolourizing and polishing agents for glass, petroleum cracking catalysts and arc-carbons, unseparated or partially separated rare earths were adequate. These applications continue till today. With the development and industrial application of powerful techniques like ion exchange and solvent extraction for the separation of rare earths, the decades after 1960 saw increasing utilization of the specific properties of the individual rare earths. Some of these advanced technological applications include: special glass for optical systems including camera lenses, phosphors for colour television, cathode ray tubes and fluorescent lighting, X-ray intensification screens, high intensity permanent magnets, electro optical devices, lasers, hydrogen storage materials, hydride rechargeable batteries, photomagnetic data storage systems, autoexhaust catalysts, special ceramics of unusual toughness, artificial diamonds and nonpoisonous plastic colorants. The topics covered in the book include rare earths: their story identity, rare earth resources, processing of ores and recovery of mixed rare earths products, separation and purification of rare earths, nonmetallic applications of rare earths, rare earth metals: production and applications, rare earth alloys and their applications, analysis of rare earth, processing of rare earth resources in India by Indian Rare Earth Ltd. and availability and market conditions

Rare earth germanates

International Nuclear Information System (INIS)

Bondar', I.A.; Vinogradova, N.V.; Dem'yanets, L.N.

1983-01-01

From the viewpoint of structural chemistry and general regularities controlling formation reactions of compounds and phases in melts, solid and gaseous states, recent achievements in the chemistry of rare earth germanates are generalized. Methods of synthesizing germanates, systems on the base of germanium oxides and rare earths are considered. The data on crystallochemical characteristics are tabulated. Individual compounds of scandium germanate are also characterized. Processes of germanate formation using the data of IR-spectroscopy, X-ray phase analysis are studied. The structure and morphotropic series of rare earth germanates and silicates are determined. Fields of their present and possible future application are considered

The Chinese Society of Rare Earth is Studying The Feasibility of Marketing Rare Earth Futures

Institute of Scientific and Technical Information of China (English)

2015-01-01

Lin Donglu,secretary-general of the Chinese Society of Rare Earth recently said,the Chinese Society of Rare Earth undertook the research on subject of the National Social Science Fund Foundation on the reform of Chinese rare earth trading pricing mechanism on promoting RMB globalization,and is focusing on studying the feasibility of marketing rare earth futures variety.

Intermetallic precipitation in rare earth-treated A413.1 alloy. A metallographic study

International Nuclear Information System (INIS)

Samuel, Agnes M.; Samuel, Fawzy H.

2018-01-01

The present study was performed mainly on A413.1 alloy. Measured amounts of La, Ce or La+Ce, Ti and Sr were added to the molten alloy in the form of master alloys. Samples sectioned from castings obtained from thermal analysis experiments were used for preparing samples for metallographic examination. The results show that addition of rare earth (RE) metals to Al-Si alloys increased the α-Al nucleation temperature and depressed the Al-Si eutectic formation temperature, thereby increasing the solidification range. Depending upon the alloying elements/additives, a large number of RE-based intermetallics could be formed: Al 4 (Ce,La), Al 13 (Ce,La) 2 Cu 3 , Al 7 (Cu,Fe) 6 (Ce,La) 6 Si 2 , Al 4 La, Al 2 La 5 Si 2 , Al 2 Ce 5 Si 2 , Al 2 (Ce,La) 5 Si 2 . Under an electron microscope, these phases appear in backscatter imaging mode in the form of thin grayish-white platelets on the dark gray Al matrix. The average thickness of these platelets is about 1.5 μm. When the alloy is grain refined with Ti-based master alloys, precipitation of a gray phase in the form of sludge is observed: Al 12 La 3 Ti 2 , or Al 12 (Ce,La) 3 Ti 2 . Regardless the alloy composition, the RE/Al ratios remain constant in each type of intermetallic. Rare earth metals have a strong affinity to react with Sr (resulting in partial modification of the eutectic Si particles) as well as some transition elements, in particular Ti and Cu. Iron has a very low affinity for interaction with RE metals. It is only confined to Fe-based intermetallics.

Intermetallic precipitation in rare earth-treated A413.1 alloy. A metallographic study

Energy Technology Data Exchange (ETDEWEB)

Samuel, Agnes M.; Samuel, Fawzy H. [Univ. du Quebec a Chicoutimi (Canada). Dept. des Sciences Appliquees; Doty, Herbert W. [General Motors, Pontiac, MI (United States). Materials Engineering; Valtierra, Salvador [Nemak, S.A., Garza Garcia (Mexico)

2018-02-15

The present study was performed mainly on A413.1 alloy. Measured amounts of La, Ce or La+Ce, Ti and Sr were added to the molten alloy in the form of master alloys. Samples sectioned from castings obtained from thermal analysis experiments were used for preparing samples for metallographic examination. The results show that addition of rare earth (RE) metals to Al-Si alloys increased the α-Al nucleation temperature and depressed the Al-Si eutectic formation temperature, thereby increasing the solidification range. Depending upon the alloying elements/additives, a large number of RE-based intermetallics could be formed: Al{sub 4}(Ce,La), Al{sub 13}(Ce,La){sub 2}Cu{sub 3}, Al{sub 7}(Cu,Fe){sub 6}(Ce,La){sub 6}Si{sub 2}, Al{sub 4}La, Al{sub 2}La{sub 5}Si{sub 2}, Al{sub 2}Ce{sub 5}Si{sub 2}, Al{sub 2}(Ce,La){sub 5}Si{sub 2}. Under an electron microscope, these phases appear in backscatter imaging mode in the form of thin grayish-white platelets on the dark gray Al matrix. The average thickness of these platelets is about 1.5 μm. When the alloy is grain refined with Ti-based master alloys, precipitation of a gray phase in the form of sludge is observed: Al{sub 12}La{sub 3}Ti{sub 2}, or Al{sub 12}(Ce,La){sub 3}Ti{sub 2}. Regardless the alloy composition, the RE/Al ratios remain constant in each type of intermetallic. Rare earth metals have a strong affinity to react with Sr (resulting in partial modification of the eutectic Si particles) as well as some transition elements, in particular Ti and Cu. Iron has a very low affinity for interaction with RE metals. It is only confined to Fe-based intermetallics.

Recovery of rare earths from used polishes by chemical vapor transport process

International Nuclear Information System (INIS)

Ozaki, T.; Machida, K.; Adachi, G.

1998-01-01

Full text: Rare earth oxide polishes are widely used in the glass industry because of its mechanical and chemical polishing action. The Japanese glass industry use 2000 tons per year of the polishes, and a large portion of them are thrown away after their polishing lifetime. A dry recovery processes for rare earths from the used polishes have been investigated by using a chemical vapor transport method via the formation of vapor complexes RAl n Cl 3+3n (R = rare earths). A flow type reactor with various temperature gradients was employed for the process. The used polishes were mixed with active carbon, and chlorinated with N 2 + Cl 2 mixture at 1273 K. Aluminium oxide were also chlorinated at lower temperature and the resulting AlCl 3 were introduced to the reactor. The rare earth chlorides and AlCl 3 were converted to the vapor complexes. These were driven along the temperature gradient, decomposed according to the reverse reaction, and regenerated RCl 3 . About 90 % of the used polish were chlorinated after 2 hours. Rare earth chlorides, AlCl 3 , and FeCl 3 were fully transported after 82 hours. The rare earth chlorides were mainly condensed over the temperature range 1263-903 K. On the other hand, AlCl 3 and FeCl 3 were deposited at the temperature range below 413 K. CaCl 2 and SrCl 2 were hardly transported and remained in the residue. When the temperature gradient with the smaller slope was used, mutual separation efficiencies among the rare earths was improved. The highest CeCl 3 purity of 80% was obtained in the process

Study of the hyperfine magnetic field acting on Ce probes substituting for the rare earth and the magnetic ordering in intermetallic compounds RAg (R=rare earth) by first principles calculations; Estudo do campo hiperfino magnetico na sonda de Ce colocada nos compostos intermetalicos do tipo RAg (R=terra rara) e do ordenamento magnetico desses compostos usando calculos de primeiros principios

Energy Technology Data Exchange (ETDEWEB)

Pereira, Luciano Fabricio Dias

2006-07-01

In this work the magnetic hyperfine field acting on Ce atoms substituting the rare-earths in R Ag compounds (R = Gd e Nd) was studied by means of first-principles electronic structure calculations. The employed method was the Augmented Plane Waves plus local orbitals (APW+lo), embodied in the WIEN2k program, within the framework of the Density Functional Theory (DFT) and with the Generalized Gradient Approximation (GGA) for the exchange and correlation potential. The super-cell approach was utilized in order to simulate for the Ce atoms acting as impurities in the R Ag matrix. In order to improve for correlation effects within the 4f shells, a Hubbard term was added to the DFT Hamiltonian, within a procedure called GGA+U. It was found that the magnetic hyperfine field (MHF) generated by the Ce 4f electron is the main component of the total MHF and that the Ce 4f ground state level is probably a combination of the m{sub l} = -2 and m{sub l} = -1 sub-levels. In addition, the ground-state magnetic structure was determined for Ho Ag and Nd Ag by observing the behavior of the total energy as a function of the lattice volume for several possible magnetic ordering in these compounds, namely, ferromagnetic, and the (0,0,{pi}), ({pi},{pi},0) and (({pi},{pi},{pi}) types of anti-ferromagnetic ordering of rare-earth atoms. It was found that the ground-state magnetic structure is anti-ferromagnetic of type ({pi},{pi},0) for both, the Ho Ag and Nd Ag compounds. The energy difference of the ferromagnetic and antiferromagnetic ordering is very small in the case of the Nd Ag compound. (author)

Structure and properties of rare earth-rich glassed for nuclear waste immobilisation

International Nuclear Information System (INIS)

Bardez, I.

2004-11-01

A new nuclear glass composition, able to immobilize highly radioactive liquid wastes from high burn-up UO 2 fuel, was established and its structure studied. The composition of the selected rare earth-rich glass is (molar %): 61.79 SiO 2 - 8.94 B 2 O 3 - 3.05 Al 2 O 3 - 14.41 Na 2 O - 6.32 CaO - 1.89 ZrO 2 - 3.60 RE 2 O 3 (with RE = La, Ce, Pr and Nd). The aim of this study was to determine the local environment of the rare earth in this glass and also to glean information about the effect of glass composition on the rare earth neighbouring (influence of Si, B, Al, Na and Ca contents). To this end, several series of glasses, prepared from the baseline glass, were studied by different characterisation methods such as EXAFS spectroscopy at the neodymium LIII-edge, optical absorption spectroscopy, Raman spectroscopy and 29 Si, 27 Al and 11 B MAS-NMR. By coupling all the results obtained, several hypotheses about the nature of the rare earth neighbouring in the glass were proposed. (author)

Fluorination of chlorocomplexes of some rare earths by xenon difluoride. [None

Energy Technology Data Exchange (ETDEWEB)

Kiselev, Yu.M.; Goryachenkov, S.A.; Martynenko, L.I. (Moskovskij Gosudarstvennyj Univ. (USSR))

1984-01-01

The results of studying the XeF/sub 2/ reaction with anhydrous hexachlorocomplexes of some RE(3) (Ce, Pr, Nd, Tb, Dy, Er, Yb) are presented. It is shown that cesium rare earth hexachlorocomplexes react with xenon difluoride at 100-400 deg C with complex formation of the Cs/sub 3/M/sup 4/F,L7 (M=Ce, Pr, Tb, Nd, Dy) composition. In case of Er and Yb under the same conditions only flouride RE derivatives corresponding to the Cs/sub 3/MF/sub 6/ formula are obtained. Possible mechanism of the process is discussed.

Novel precursors for the deposition of rare earth oxides

International Nuclear Information System (INIS)

Ahlers, Mareike

2010-01-01

orthoformate, were not fully replaced by the trimethyl orthoformate molecules. The thermal decomposition yield the respective rare earth oxide chloride REOCl (RE = Sm, Eu) and is divided into three endothermic steps followed by an exothermic step. Presumably, the compounds first lose the solvent molecules in multiple steps followed by a decomposition of the solvent free RE(ClO 4 ) 3 . Three different structure types have been determined for the dimethoxyethane solvates of the rare earth perchlorates, corresponding to the lanthanide ion radii. For the lighter rare earth elements the compound [RE(ClO 4 ) 2 (O 2 C 4 H 10 ) 3 ](ClO 4 ) (RE = La, Eu) was synthesized and characterized. Non coordinating perchlorate anions exist alongside the complex [RE(ClO 4 ) 2 (O 2 C 4 H 10 ) 3 ] + cation. In addition, RE(ClO 4 ) 2 (O 2 C 4 H 10 ) 2 (RE = Pr, Nd) was obtained, analogue to the respective nitrates. [RE(ClO 4 ) 2 (O 2 C 4 H 10 ) 3 ](ClO 4 )(O 2 C 4 H 10 ) 0.5 (RE = Er, Lu) was found for the heavier rare earth elements, which contains further non coordinated solvent molecules in contrast to the first structure type. The thermal decomposition is dominated by the typical exothermic step as well. The residue is either the respective rare earth oxide chloride REOCl (RE = La, Pr, Eu), or cubic rare earth oxide RE 2 O 3 (RE = Nd, Er, Lu). The known structure type of the perchlorate tetrahydrofuran was expanded with the compound RE(ClO 4 ) 4 (OC 4 H 8 ) 4 (RE = Ce, Sm, Er, Lu). The orthorhombic modification for the heavier rare earth elements erbium and lutetium were also obtained. [Sc(ClO 4 )(OMe)(OC 4 H 8 ) 4 ](ClO 4 ) was structurally characterized using a completely new ionic structure type and analyzed thermally. The thermal decomposition is again dominated by an intense exothermic step. Contrary to the dimethoxyethane solvates, the respective rare earth oxide RE 2 O 3 (RE = Er, Lu) and CeO 2 or the oxide chloride SmOCl is the remaining residue.

Rare earth minerals and resources in the world

Energy Technology Data Exchange (ETDEWEB)

Kanazawa, Yasuo [Human Resource Department, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Umezono, Tsukuba 305-8568 (Japan)]. E-mail: y.kanazawa@aist.go.jp; Kamitani, Masaharu [Institute for Geo-Resources and Environment, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8567 (Japan)

2006-02-09

About 200 rare earth (RE) minerals are distributed in a wide variety of mineral classes, such as halides, carbonates, oxides, phosphates, silicates, etc. Due to the large ionic radii and trivalent oxidation state, RE ions in the minerals have large coordination numbers (c.n.) 6-10 by anions (O, F, OH). Light rare earth elements (LREEs) tend to occupy the larger sites of 8-10 c.n. and concentrate in carbonates and phosphates. On the other hand, heavy rare earth elements (HREEs) and Y occupy 6-8 c.n. sites and are abundant in oxides and a part of phosphates. Only a few mineral species, such as bastnaesite (Ce,La)(CO{sub 3})F, monazite (Ce,La)PO{sub 4}, xenotime YPO{sub 4}, and RE-bearing clay have been recovered for commercial production. Bayan Obo, China is the biggest RE deposit in the world. One of probable hypotheses for ore geneses is that the deposit might be formed by hydrothermal replacement of carbonate rocks of sedimentary origin. The hydrothermal fluid may be derived from an alkaline-carbonatite intrusive series. Following Bayan Obo, more than 550 carbonatite/alkaline complex rocks constitute the majority of the world RE resources. The distribution is restricted to interior and marginal regions of continents, especially Precambrian cratons and shields, or related to large-scale rift structures. Main concentrated areas of the complexes are East African rift zones, northern Scandinavia-Kola peninsula, eastern Canada and southern Brazil. Representative sedimentary deposits of REE are placer- and conglomerate-types. The major potential countries are Australia, India, Brazil, and Malaysia. Weathered residual deposits have been formed under tropical and sub-tropical climates. Bauxite and laterite nickel deposit are the representative. Ion adsorption clay without radioactive elements is known in southern China. Weathering processes concentrate REE in a particular clay mineral-layer in the weathered crusts whose source were originally REE-rich rocks like granite

Rare earth minerals and resources in the world

International Nuclear Information System (INIS)

Kanazawa, Yasuo; Kamitani, Masaharu

2006-01-01

About 200 rare earth (RE) minerals are distributed in a wide variety of mineral classes, such as halides, carbonates, oxides, phosphates, silicates, etc. Due to the large ionic radii and trivalent oxidation state, RE ions in the minerals have large coordination numbers (c.n.) 6-10 by anions (O, F, OH). Light rare earth elements (LREEs) tend to occupy the larger sites of 8-10 c.n. and concentrate in carbonates and phosphates. On the other hand, heavy rare earth elements (HREEs) and Y occupy 6-8 c.n. sites and are abundant in oxides and a part of phosphates. Only a few mineral species, such as bastnaesite (Ce,La)(CO 3 )F, monazite (Ce,La)PO 4 , xenotime YPO 4 , and RE-bearing clay have been recovered for commercial production. Bayan Obo, China is the biggest RE deposit in the world. One of probable hypotheses for ore geneses is that the deposit might be formed by hydrothermal replacement of carbonate rocks of sedimentary origin. The hydrothermal fluid may be derived from an alkaline-carbonatite intrusive series. Following Bayan Obo, more than 550 carbonatite/alkaline complex rocks constitute the majority of the world RE resources. The distribution is restricted to interior and marginal regions of continents, especially Precambrian cratons and shields, or related to large-scale rift structures. Main concentrated areas of the complexes are East African rift zones, northern Scandinavia-Kola peninsula, eastern Canada and southern Brazil. Representative sedimentary deposits of REE are placer- and conglomerate-types. The major potential countries are Australia, India, Brazil, and Malaysia. Weathered residual deposits have been formed under tropical and sub-tropical climates. Bauxite and laterite nickel deposit are the representative. Ion adsorption clay without radioactive elements is known in southern China. Weathering processes concentrate REE in a particular clay mineral-layer in the weathered crusts whose source were originally REE-rich rocks like granite and

Safety aspects in rare earths recovery

International Nuclear Information System (INIS)

Bhattacharya, R.

2014-01-01

Recovery of rare earths involves mining of beach sands, mineral separation to obtain monazite and its chemical processing to obtain rare earth composites. The composites are then subjected to further chemical treatment to obtain individual rare earths. Although the separated out rare earths are not radioactive, the process for recovery of rare earths involve both radiological as well as conventional hazards. This paper highlights the safety aspects in the mining, mineral separation and chemical processing of monazite to obtain rare earths

Synthesis and luminescence studies of novel rare earth activated lanthanum pentaborate

International Nuclear Information System (INIS)

Nagpure, P.A.; Bajaj, N.S.; Omanwar, S.K.; Sonekar, R.P.

2011-01-01

The lanthanum pentaborate (LaB 5 O 9 ) is a novel material which exhibits excellent luminescence when doped with rare earth ions. It was prepared by a novel technique which is a slight variation of solution combustion synthesis. The synthesis is based on the exothermic reaction between the fuel (urea) and oxidizer (ammonium nitrate). The structure of the prepared material was confirmed by powder XRD technique. The photoluminescence of rare earth ions (Ce 3+ , Eu 3+ ) and sensitized luminescence of Gd 3+ (Pr 3+ -Gd 3+ and Bi 3+ -Gd 3+ ) in LaB 5 O 9 have been studied. LaB 5 O 9 :Ce 3+ shows broad band UV emission at 317 nm and LaB 5 O 9 :Eu 3+ shows orange red emission. LaB 5 O 9 : Pr 3+ -Gd 3+ and LaB 5 O 9 : Bi 3+ -Gd 3+ exhibit efficient luminescence of Gd 3+ in narrow UVB region at 310 nm. The material (La 0.5 Pr 0.4 )B 5 O 9 :Gd 0.1 exhibits intense narrow band UVB emission at 310 nm and could be a potential candidate for UVB phosphors used in phototherapy lamps. (author)

Rare earth conversion coating on Mg-8.5Li alloys

International Nuclear Information System (INIS)

Yang Xiaowei; Wang Guixiang; Dong Guojun; Gong Fan; Zhang Milin

2009-01-01

The conversion coating formed by immersion in a solution containing rare earth salt on Mg-8.5Li alloy was studied and the corrosion resistance was evaluated as well. The surface morphology was observed by scanning electron microscopy (SEM), and the chemical composition was characterized by X-ray photoelectron spectroscopy (XPS). The corrosion behaviors of Mg-8.5Li alloy and conversion coating were assessed by means of potentiodynamic polarization curves, electrochemical impedance spectra (EIS) and immersion tests. The experimental results indicated that the coating with cracked morphology was homogeneous. It was mainly composed of La 2 O 3 , CeO 2 , Mn 2 O 3 and MnO 2 as detected by XPS. The results of electrochemical measurements and immersion tests revealed that the rare earth conversion coating possessed better corrosion resistance than bare alloy and chromate conversion coating.

China's Rare Earth Supply Chain: Illegal Production, and Response to new Cerium Demand

Science.gov (United States)

Nguyen, Ruby Thuy; Imholte, D. Devin

2016-07-01

As the demand for personal electronic devices, wind turbines, and electric vehicles increases, the world becomes more dependent on rare earth elements. Given the volatile, Chinese-concentrated supply chain, global attempts have been made to diversify supply of these materials. However, the overall effect of supply diversification on the entire supply chain, including increasing low-value rare earth demand, is not fully understood. This paper is the first attempt to shed some light on China's supply chain from both demand and supply perspectives, taking into account different Chinese policies such as mining quotas, separation quotas, export quotas, and resource taxes. We constructed a simulation model using Powersim Studio that analyzes production (both legal and illegal), production costs, Chinese and rest-of-world demand, and market dynamics. We also simulated new demand of an automotive aluminum-cerium alloy in the US market starting from 2018. Results showed that market share of the illegal sector has grown since 2007-2015, ranging between 22% and 25% of China's rare earth supply, translating into 59-65% illegal heavy rare earths and 14-16% illegal light rare earths. There will be a shortage in certain light and heavy rare earths given three production quota scenarios and constant demand growth rate from 2015 to 2030. The new simulated Ce demand would require supply beyond that produced in China. Finally, we illustrate revenue streams for different ore compositions in China in 2015.

Recycling of rare earths from Hg-containing fluorescent lamp scraps by solid state chlorination

International Nuclear Information System (INIS)

Lorenz, Tom; Froehlich, Peter; Bertau, Martin; Golon, Katja

2015-01-01

Solid state chlorination with NH 4 Cl comprises a method for rare earth recycling apart from pyro- or hydrometallurgical strategies. The examined partially Hg-containing fluorescent lamp scraps are rich in rare earths like La, Ce, Tb and Gd, but especially in Y and Eu. By mixing with NH 4 Cl and heating up to NH 4 Cl decomposition temperature in a sublimation reactor, Y and Eu could be transferred selectively into their respective metal chlorides with high yields. The yield and selectivity depend on temperature and the ratio of NH 4 Cl to fluorescent lamp scraps, which were varied systematically.

Double Solvent for Extracting Rare Earth Concentrate

International Nuclear Information System (INIS)

Bintarti, AN; Bambang EHB

2007-01-01

An extraction process to rare earth concentrate which contain elements were yttrium (Y), lanthanum (La), cerium (Ce), neodymium (Nd), samarium (Sm), gadolinium (Gd) and dysprosium (Dy) which were dissolved in to nitric acid has been done. The experiment of the extraction by double solvent in batch to mix 10 ml of the feed with 10 ml solvent contained the pair of solvent was TBP and TOA, D2EHPA and TOA, TBP and D2EHPA in cyclohexane as tinner. It was selected a right pairs of solvent for doing variation such as the acidity of the feed from 2 - 6 M and the time of stirring from 5 - 25 minutes gave the good relatively extraction condition to Dy element such as using 10 % volume of TOA in D2EHPA and cyclohexane, the acidity of the feed 3 M and the time stirring 15 minutes produced coefficient distribution to dysprosium = 0.586 and separation factor Dy-Ce = ∼ (unlimited); Dy-Nd = 4.651. (author)

The lattice dynamical studies of rare earth compounds: electron-phonon interactions

International Nuclear Information System (INIS)

Jha, Prafulla K.; Sanyal, Sankar P.; Singh, R.K.

2002-01-01

During the last two decades chalcogenides and pnictides of rare earth (RE) atoms have drawn considerable attention of the solid state physicists because of their peculiar electronic, magnetic, optical and phonon properties. Some of these compounds e.g. sulphides and selenides of cerium (Ce), samarium (Sm), yttrium (Y), ytterbium (Yb), europium (Eu) and thulium (Tm) and their alloys show nonintegral valence (between 2 and 3), arising due to f-d electron hybridization at ambient temperature and pressure. The rare earth mixed valence compounds (MVC) reviewed in this article crystallize in simple cubic structure. Most of these compounds show the existence of strong electron-phonon coupling at half way to the zone boundary. This fact manifests itself through softening of the longitudinal acoustic mode, negative value of elastic constant C 12 etc. The purpose of this contribution is to review some of the recent activities in the fields of lattice dynamics and allied properties of rare earth compounds. The present article is primarily devoted to review the effect of electron-phonon interactions on the dynamical properties of rare earth compounds by using the lattice dynamical model theories based on charged density deformations and long-range many body forces. While the long range charge transfer effect arises due to f-d hybridization of nearly degenerate 4f-5d bands of rare earth ions, the density deformation comes into the picture of breathing motion of electron shells. These effects of charge transfer and charge density deformation when considered in the lattice dynamical models namely the three body force rigid ion model (TRM) and breathing shell model (BSM) are quite successful in explaining the phonon anomalies in these compounds and undoubtedly unraveled many important physical process governing the phonon anomalies in rare earth compounds

Determination of free boron in rare earth hexaborides

International Nuclear Information System (INIS)

Kugaj, L.N.; Nazarchuk, T.N.

1975-01-01

The method of N.I. Timofeeva et al. (1968) for the determination of free B in rare earth hexaborides was modified by replacing the 1:10 HNO 3 by nonoxidizing 2:1 or 3:1 H 2 SO 4 to dissolve the hexaborides and leave free B in the residue. A sample of 0.5-1.0 g rare earth hexaboride was heated in 50-80 ml 3:1 H 2 SO 4 at 210 0 for 2 hr, and the cool solutions was diluted. The residue containing free B and B 4 C was filtered, rinsed, and heated in dilute HNO 3 at mild temperature for 15-20 min. The filtrate was separated from insoluble B 4 C, neutralized with 10% NaOH, and H 3 BO 3 was titrated with NaOH in the presence of inverted sugar vs. phenophthalein. The free B content was underestimated by less than or equal to 4.3% in nearly all cases. The proposed technique is applicalbe to hexaborides of La, Y, Ce, Pr, Nd, Sm, Gd, and Eu

Chemiluminescent Diagnostics of Free-Radical Processes in an Abiotic System and in Liver Cells in the Presence of Nanoparticles Based on Rare-Earth Elements nReVO4:Eu3+ (Re = Gd, Y, La) and CeO2

Science.gov (United States)

Averchenko, E. A.; Kavok, N. S.; Klochkov, V. K.; Malyukin, Yu. V.

2014-11-01

We have used luminol-dependent chemiluminescence with Fenton's reagent to study the effect of nanoparticles based on rare-earth elements of different sizes and shapes on free-radical processes in abiotic and biotic cell-free systems, and also in isolated cells in vitro. We have estimated the effects of rare-earth orthovanadate nanoparticles of spherical (GdYVO4:Eu3+, 1-2 nm), spindle-shaped (GdVO4:Eu3+, 25 ×8 nm), and rod-shaped (LaVO4:Eu3+, 57 × (6-8) nm) nanoparticles and spherical CeO2 nanoparticles (sizes 1-2 nm and 8-10 nm). We have shown that in contrast to the abiotic system, in which all types of nanoparticles exhibit antiradical activity, in the presence of biological material, extra-small spherical (1-2 nm) nanoparticles of both types exhibit pro-oxidant activity, and also enhance pro-oxidant induced oxidative stress (for the pro-oxidants hydrogen peroxide and tert-butyl hydroperoxide). The effect of rare-earth orthovanadate spindle and rod shaped nanoparticles in this system was neutral; a moderate antioxidant effect was exhibited by 8-10 nm CeO2 nanoparticles.

Separation of rare earth elements in monazite sand by anion exchange resin (pt. II)

International Nuclear Information System (INIS)

Cha, K.W.; Lee, J.H.; Yoon, S.H.; Ha, Y.G.

1980-01-01

An anion exchange method for separating Y, La, Ce, Pr, and Nd element in monazaites and into enriched fractions has been developed. The complexed rare earth ions with EDTA at pH 8.4 passed through the resin column of the various size and eluted with 0.0301 M EDTA as eluent at flow rate of 1 ml/min and 2 ml/min. The result of separation is good in the high column length rather than the low on using the resin of the same amount and the volume of eluent required in eluting all the rare earths at 2 ml/min flow rare is larger than that at 1 ml/min and the result of separation obtained here is unsatisfactory. (author)

A combinatorial matrix of rare earth chloride mixtures as corrosion inhibitors of AA2024-T3: Optimisation using potentiodynamic polarisation and EIS

International Nuclear Information System (INIS)

Muster, T.H.; Sullivan, H.; Lau, D.; Alexander, D.L.J.; Sherman, N.; Garcia, S.J.; Harvey, T.G.; Markley, T.A.; Hughes, A.E.; Corrigan, P.A.; Glenn, A.M.; White, P.A.; Hardin, S.G.; Mardel, J.; Mol, J.M.C.

2012-01-01

A combinatorial matrix of four rare earth chlorides has been evaluated for the corrosion inhibition of aluminium alloy AA2024-T3 in aqueous solution. Two electrochemical techniques, potentiodynamic polarisation (PP) and electrochemical impedance spectroscopy (EIS), were used to evaluate AA2024-T3 corrosion in 0.1 M NaCl with the addition of 10 −3 M of rare earth chloride mixtures at time periods up to 18 h. PP experiments showed rare earth inhibition of up to 98% within the first hour and thereafter corrosion rates were steadily decreased. The open-circuit potential (OCP) of AA2024-T3 decreased as a function of time for all solutions indicating predominantly cathodic inhibition. However, differing trends in the OCP were observed during PP and EIS experiments and are discussed in terms of likely time-dependent mechanisms. A comparative study of optimisation models indicated the best mixture at 10 −3 M total inhibitor concentration was predicted to be 72% cerium (Ce) and 28% (praseodymium (Pr)/lanthanum (La)) ions. As the amount of Ce is decreased from this level the corrosion inhibition is predicted to decrease also, regardless of what other rare earths (La, Pr and Nd) are added alone or in combination. Individually, La, Pr and Nd show varying levels of corrosion inhibition activity, all of which are inferior to that of Ce. If Ce is absent entirely, then a mixture of approximately 50% Pr and 50% Nd is predicted to be preferred. This is one of the first applications of combinatorial design for the optimisation of corrosion inhibitor mixtures.

ICP-AES determination of rare earths in zirconium with prior chemical separation of the matrix

International Nuclear Information System (INIS)

Rajeswari, B.; Dhawale, B.A.; Page, A.G.; Sastry, M.D.

2002-01-01

Zirconium being one of the most important material in nuclear industry used as a fuel cladding in reactors and an additive in advanced fuels necessitates its characterization for trace metallic contents. Zirconium, as refractory in nature as the rare earth elements, has a complex spectrum comprising of several emission lines. Rare earths, which are high neutron absorbers have to be analysed at very low limits. Hence, to achieve the desired limits, the major matrix has to be separated prior to rare earth determination. The present paper describes the method developed for the separation of rare earths from zirconium by solvent extraction using Trioctyl Phosphine Oxide (TOPO) as the extractant followed by their determination using Inductively Coupled Plasma - Atomic Emission Spectrometric (ICP-AES) method. Initially, radiochemical studies were carried out using known amounts of gamma active tracers of 141 Ce, 152-154 Eu, 153 Gd and 95 Zr for optimisation of extraction conditions using Tl- activated NaI detector. The optimum conditions at 0.5 M TOPO/xylene in 6 M HCl so as to achieve a quantitative recovery of rare earth analytes alongwith a near total extraction of zirconium in the organic phase, was further extended to carry out the studies using ICP-AES method. The recovery of rare earths was found to be quantitative within experimental error with a precision better than 10% RSD. (author)

Metallothermic reduction of rare earth oxides

International Nuclear Information System (INIS)

Sharma, R.A.

1986-01-01

Rare earth oxides can be reduced to rare earth metals by a novel, high yield, metallothermic process. The oxides are dispersed in a suitable, molten, calcium chloride bath along with sodium metal. The sodium reacts with the calcium chloride to produce calcium metal which reduces the rare earth oxides to rare earth metals. The metals are collected in a discrete layer in the reaction vessel

Rare earth industries: Downstream business

International Nuclear Information System (INIS)

2011-01-01

The value chain of the rare earths business involves mining, extraction, processing, refining and the manufacture of an extensive range of downstream products which find wide applications in such industries including aerospace, consumer electronics, medical, military, automotive, renewable wind and solar energy and telecommunications. In fact the entire gamut of the high-tech industries depends on a sustainable supply of rare earths elements. The explosive demand in mobile phones is an excellent illustration of the massive potential that the rare earths business offers. In a matter of less than 20 years, the number of cell phones worldwide has reached a staggering 5 billion. Soon, going by the report of their growth in sales, the world demand for cell phones may even exceed the global population. Admittedly, the rare earths business does pose certain risks. Top among the risks are the health and safety risks. The mining, extraction and refining of rare earths produce residues and wastes which carry health and safety risks. The residues from the extraction and refining are radioactive, while their effluent waste streams do pose pollution risks to the receiving rivers and waterways. But, as clearly elaborated in a recent report by IAEA experts, there are technologies and systems available to efficiently mitigate such risks. The risks are Rare Earth manageable. However, it is crucial that the risk and waste management procedures are strictly followed and adhered to. This is where effective monitoring and surveillance throughout the life of all such rare earths facilities is crucial. Fortunately, Malaysia's regulatory standards on rare earths follow international standards. In some areas, Malaysia's regulatory regime is even more stringent than the international guidelines. (author)

Rare earth industries: Strategies for Malaysia

International Nuclear Information System (INIS)

2011-01-01

Evidently, many reports cite Malaysia as having reasonably substantial amounts of rare earths elements. In fact, based on the rare earths found in the residual tin deposits alone, Malaysia has about 30,000 tonnes. This does not take into account unmapped deposits which experts believe may offer more tonnages of rare earths. Brazil which is reported to have about 48,000 tonnes has announced plans to invest aggressively in the rare earths business. China has on record the largest reserves with about 36 million tonnes. This explains why China has invested heavily in the entire value chain of the rare earths business. Chinas committed investment in rare earths started many years ago when the country's foremost leaders proclaimed the strategic position of rare earths in the world economy. That forecast is now a reality where the rise in the green high-tech economy is seen driving global demand for rare earths in a big way. Malaysia needs to discover and venture into new economic growth areas. This will help fuel the country's drive to achieve a high income status by 2020 as articulated in the New Economic Model (NEM) and the many supporting Economic Transformation Plans that the Government has recently launched. Rare earths may be the new growth area for Malaysia. However, the business opportunities should not just be confined to the mining, extraction and production of rare earths elements alone if Malaysia is to maximise benefits from this industry. The industry's gold mine is in the downstream products. This is also the sector that China wants to expand. Japan which now controls about 50 % of the global market for downstream rare earths-based high-tech components is desperately looking for partners to grow their stake in the business. Malaysia needs to embark on the right strategies in order to build the rare earths industry in the country. What are the strategies? (author)

Microstructural characterisation of Al-Si cast alloys containing rare earth additions

Science.gov (United States)

Elgallad, E. M.; Ibrahim, M. F.; Doty, H. W.; Samuel, F. H.

2018-05-01

This paper presents a thorough study on the effect of rare earth elements, specifically La and Ce, on the microstructure characteristics of non-modified and Sr-modified A356 and A413 alloys. Several alloys were prepared by adding 1% La and 1% Ce either individually or in combination. Microstructural characterisation was carried out using optical microscopy, scanning electron microscopy and electron probe microanalysis as well as differential scanning calorimetry (DSC) analysis. The results showed that the individual and combined additions of La and Ce did not bring about any modification or even refinement in the eutectic Si structure. Moreover, these additions were found to negate the modification effect of Sr, particularly in the presence of La. The A356 and A413 alloys containing La and/or Ce displayed high phase volume fractions owing to the formation of Al-Si-La/Ce/(La,Ce) and Al-Ti-La/Ce intermetallic phases. DSC analysis revealed that the formation temperatures of these phases varied from 560 to 568 °C and 568 to 574 °C, respectively. This analysis also showed that the addition of La and Ce whether individually or in combination resulted in a depression in the eutectic temperature and a considerable increase in the solidification range, particularly for the A413 alloy.

Rare earth-iron-boron premanent magnets

International Nuclear Information System (INIS)

Ghendehari, M.H.

1988-01-01

This patent describes a method for producing rare earth-iron-boron permanent magnets containing added rare earth oxide, comprising the steps of: (a) mixing a particulate alloy containing at least one rare earth metal, iron, and boron with at least one particulate rare earth oxide; (b) aligning magnetic domains of the mixture in a magnetic field; (c) compacting the aligned mixture to form a shape; and (d) sintering the compacted shape

Process optimization and kinetics for leaching of rare earth metals from the spent Ni-metal hydride batteries.

Science.gov (United States)

Meshram, Pratima; Pandey, B D; Mankhand, T R

2016-05-01

Nickel-metal hydride batteries (Ni-MH) contain not only the base metals, but valuable rare earth metals (REMs) viz. La, Sm, Nd, Pr and Ce as well. In view of the importance of resource recycling and assured supply of the contained metals in such wastes, the present study has focussed on the leaching of the rare earth metals from the spent Ni-MH batteries. The conditions for the leaching of REMs from the spent batteries were optimized as: 2M H2SO4, 348K temperature and 120min of time at a pulp density (PD) of 100g/L. Under this condition, the leaching of 98.1% Nd, 98.4% Sm, 95.5% Pr and 89.4% Ce was achieved. Besides the rare earth metals, more than 90% of base metals (Ni, Co, Mn and Zn) were also leached out in this condition. Kinetic data for the dissolution of all the rare earth metals showed the best fit to the chemical control shrinking core model. The leaching of metals followed the mechanism involving the chemical reaction proceeding on the surface of particles by the lixiviant, which was corroborated by the XRD phase analysis and SEM-EDS studies. The activation energy of 7.6, 6.3, 11.3 and 13.5kJ/mol was acquired for the leaching of neodymium, samarium, praseodymium and cerium, respectively in the temperature range 305-348K. From the leach liquor, the mixed rare earth metals were precipitated at pH∼1.8 and the precipitated REMs was analyzed by XRD and SEM studies to determine the phases and the morphological features. Copyright © 2015. Published by Elsevier Ltd.

Development of novel rare earth doped fluoride and oxide scintillators for two-dimensional imaging

Czech Academy of Sciences Publication Activity Database

Yoshikawa, A.; Yanagida, T.; Yokota, Y.; Kamada, K.; Kawaguchi, N.; Fukuda, K.; Yamazaki, A.; Watanabe, K.; Uritani, A.; Iguchi, T.; Boulon, G.; Nikl, Martin

2011-01-01

Roč. 29, č. 12 (2011), s. 1178-1182 ISSN 1002-0721 Grant - others:AV ČR(CZ) M100100910 Institutional research plan: CEZ:AV0Z10100521 Keywords : scintillator * gamma-ray detection * neutron detection * fluoride * Ce * Eu * rare earth Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.901, year: 2011

Chemical analysis of rare earth elements

International Nuclear Information System (INIS)

Tsukahara, Ryoichi; Sakoh, Takefumi; Nagai, Iwao

1994-01-01

Recently attention has been paid to ICP-AES or ICP-MS, and the reports on the analysis of rare earth elements by utilizing these methods continue to increase. These reports have become to take about 30% of the reports on rare earth analysis, and this is because these methods are highly sensitive to rare earth elements, and also these methods have spread widely. In ICP-AES and ICP-MS, mostly solution samples are measured, therefore, solids must be made into solution. At the time of quantitatively determining the rare earth elements of low concentration, separation and concentration are necessary. Referring to the literatures reported partially in 1990 and from 1991 to 1993, the progress of ICP-AES and ICP-MS is reported. Rare earth oxides and the alloys containing rare earth elements are easily decomposed with acids, but the decomposition of rocks is difficult, and its method is discussed. The separation of the rare earth elements from others in geochemical samples, cation exchange process is frequently utilized. Also solvent extraction process has been studied. For the separation of rare earth elements mutually, chromatography is used. The spectral interference in spectral analysis was studied. The comparison of these methods with other methods is reported. (K.I)

Improving soft magnetic properties of Mn-Zn ferrite by rare earth ions doping

Science.gov (United States)

Zhong, X. C.; Guo, X. J.; Zou, S. Y.; Yu, H. Y.; Liu, Z. W.; Zhang, Y. F.; Wang, K. X.

2018-04-01

Mn-Zn ferrites doped with different Sm2O3, Gd2O3, Ce2O3 or Y2O3 were prepared by traditional ceramic technology using industrial pre-sintered powders. A small amount of Sm2O3, Gd2O3, Ce2O3 or Y2O3 can significantly improve the microstructure and magnetic properties. The single spinel phase structure can be maintained with the doping amount up to 0.07 wt.%. A refined grain structure and uniform grain size distribution can be obtained by doping. For all rare earth oxides, a small amount of doping can significantly increase the permeability and reduce the coercivity and magnetic core loss. The optimized doping amount for Sm2O3 or Gd2O3 is 0.01 wt.%, while for Ce2O3 or Y2O3 is 0.03 wt.%. A further increase of the doping content will lead to reduced soft magnetic properties. The ferrite sample with 0.01 wt.% Sm2O3 exhibits the good magnetic properties with permeability, loss, and coercivity of 2586, 316 W/kg, and 24A/m, respectively, at 200 mT and 100 kHz. The present results indicate that rare earth doping can be suggested to be one of the effective ways to improve the performance of soft ferrites.

Improving soft magnetic properties of Mn-Zn ferrite by rare earth ions doping

Directory of Open Access Journals (Sweden)

X. C. Zhong

2018-04-01

Full Text Available Mn-Zn ferrites doped with different Sm2O3, Gd2O3, Ce2O3 or Y2O3 were prepared by traditional ceramic technology using industrial pre-sintered powders. A small amount of Sm2O3, Gd2O3, Ce2O3 or Y2O3 can significantly improve the microstructure and magnetic properties. The single spinel phase structure can be maintained with the doping amount up to 0.07 wt.%. A refined grain structure and uniform grain size distribution can be obtained by doping. For all rare earth oxides, a small amount of doping can significantly increase the permeability and reduce the coercivity and magnetic core loss. The optimized doping amount for Sm2O3 or Gd2O3 is 0.01 wt.%, while for Ce2O3 or Y2O3 is 0.03 wt.%. A further increase of the doping content will lead to reduced soft magnetic properties. The ferrite sample with 0.01 wt.% Sm2O3 exhibits the good magnetic properties with permeability, loss, and coercivity of 2586, 316 W/kg, and 24A/m, respectively, at 200 mT and 100 kHz. The present results indicate that rare earth doping can be suggested to be one of the effective ways to improve the performance of soft ferrites.

The industry of metallic rare earths (R.E.)

International Nuclear Information System (INIS)

Poirier, P.

1979-01-01

The following subjects are discussed: rare earths resources (rare earths abondance and world reserves, main ores). Rare earths separation and purification (ionic exchange, solvent extraction). Metallic rare earths and their mixtures, metallothermic reduction of oxides or fluorides (Ca, Mg, Al, Si or rare earth metals), Co-reduction process for intermetallic compounds (SmCo 5 ). Industrial applications of metallic rare earths (traditional applications such as flints, nodular cast iron, steel refining, magnesium industrie, applications under development such as rare earths/cobalt magnets, LaNi 5 for hydrogen storage, special alloys (automotive post combustion), magnetostrictive alloys). Economical problems: rare earth are elements relatively abundant and often at easily accessible prices. However, this group of 15 elements are liable to certain economical restraints. It is difficult to crack ore for only one rare earth. Availability of one given rare earth must be associated with the other corresponding rare earths to absorb all the other rare earths in other applications. Rare-earth industry has a strong expanding rate. 20% per year average for 6 years with Rhone-Poulenc. Thanks to their exceptional, specific characteristics rare earths have a bright future particularly for their metals

Preparation and characterization of PT-rare earth/C electrocatalysts for PEM fuel cells

International Nuclear Information System (INIS)

Santoro, Thais Aranha de Barros

2009-01-01

Pt-rare earth/C electrocatalysts (rare earth = La, Ce, Pr, Nd, Sm, Tb, Dy, Ho, Er, Tm, and Lu) were prepared (20 wt.% and Pt-to-RE atomic ratio of 50:50) by an alcohol reduction process using H 2 PtCl 6 .6H 2 O (Aldrich) and rare earth (III) chlorides (Aldrich) as metal sources, ethylene glycol as solvent and reducing agent, and Vulcan XC72 as support. The electrocatalysts were characterized by Energy Dispersive X-ray Spectroscopy (EDX), X-Ray Diffractometry (XRD) and Transmission Electron Microscopy (TEM). The energy dispersive x-ray spectroscopy analysis showed that the Pt-Rare Earth atomic ratios obtained for all electrocatalysts were similar to those used in the preparations. In all diffractograms, it was observed a broad peak at about 25 degree which was associated to the Vulcan XC72 support material and four peaks at approximately 28=40 degree, 47 degree, 67 degree and 82 degree, which were associated to the (111), (200), (220), (311), and (222) planes, respectively, of the face-centered cubic (fcc) structure characteristic of platinum and platinum alloys. For the Pt-Rare Earth/C electrocatalysts, it was also observed peaks related to the rare earth oxides on the X ray diffractograms. PtLa/C electrocatalysts were prepared at different atomic ratio. Transmission electronic microscopy micrographs of electrocatalysts showed a reasonable distribution of the Pt particles on the carbon support with some agglomerations, which is in agreement with x-ray diffractometry result. The performance for CO, methanol and ethanol oxidation was investigated by cyclic voltammetry, chronoamperometry and Fourier transform infrared spectroscopy spectroscopy. The electrocatalytic activity of the Pt-Rare Earth/C electro catalyst, specially PtLa/C, were higher than that of the Pt/C electrocatalyst. Fourier transform infrared spectroscopy studies for ethanol oxidation on Pt-Rare Earth/C electrocatalyst showed that acetaldehyde and acetic acid were the main products. The PtLa/C (30

Determination of free boron in rare earth hexaborides

Energy Technology Data Exchange (ETDEWEB)

Kugai, L N; Nazarchuk, T N [AN Ukrainskoj SSR, Kiev. Inst. Problem Materialovedeniya

1975-06-01

The method of N.I. Timofeeva et al. (1968) for the determination of free B in rare earth hexaborides was modified by replacing the 1:10 HNO/sub 3/ by nonoxidizing 2:1 or 3:1 H/sub 2/SO/sub 4/ to dissolve the hexaborides and leave free B in the residue. A sample of 0.5-1.0 g rare earth hexaboride was heated in 50-80 ml 3:1 H/sub 2/SO/sub 4/ at 210/sup 0/ for 2 hr, and the cool solution was diluted. The residue containing free B and B/sub 4/C was filtered, rinsed, and heated in dilute HNO/sub 3/ at mild temperature for 15-20 min. The filtrate was separated from insoluble B/sub 4/C, neutralized with 10% NaOH, and H/sub 3/BO/sub 3/ was titrated with NaOH in the presence of inverted sugar vs. phenophthalein. The free B content was underestimated by less than or equal to 4.3% in nearly all cases. The proposed technique is applicalbe to hexaborides of La, Y, Ce, Pr, Nd, Sm, Gd, and Eu.

Rare earth elements: end use and recyclability

Science.gov (United States)

Goonan, Thomas G.

2011-01-01

Rare earth elements are used in mature markets (such as catalysts, glassmaking, lighting, and metallurgy), which account for 59 percent of the total worldwide consumption of rare earth elements, and in newer, high-growth markets (such as battery alloys, ceramics, and permanent magnets), which account for 41 percent of the total worldwide consumption of rare earth elements. In mature market segments, lanthanum and cerium constitute about 80 percent of rare earth elements used, and in new market segments, dysprosium, neodymium, and praseodymium account for about 85 percent of rare earth elements used. Regardless of the end use, rare earth elements are not recycled in large quantities, but could be if recycling became mandated or very high prices of rare earth elements made recycling feasible.

Hydrothermal synthesis, characterization and up/down-conversion luminescence of barium rare earth fluoride nanocrystals

International Nuclear Information System (INIS)

Jia, Li-Ping; Zhang, Qiang; Yan, Bing

2014-01-01

Graphical abstract: Lanthanide ions doped bare earth rare earth fluoride nanocrystals are synthesized by hydrothermal technology and characterized. The down/up-conversion luminescence of them are discussed. - Highlights: • Mixed hydrothermal system H 2 O–OA (EDA)–O-A(LO-A) is used for synthesis. • Barium rare earth fluoride nanocrystals are synthesized comprehensively. • Luminescence for down-conversion and up-conversion are obtained for these systems. - Abstract: Mixed hydrothermal system H 2 O–OA (EDA)–O-A(LO-A) is developed to synthesize barium rare earth fluorides nanocrystals (OA = oleylamine, EDA = ethylenediamine, O-A = oleic acid and LO-A = linoleic acid). They are presented as BaREF 5 (RE = Ce, Pr, Nd, Eu, Gd, Tb, Dy, Y, Tm, Lu) and Ba 2 REF 7 (RE = La, Sm, Ho, Er, Yb). The influence of reaction parameters (rare earth species, hydrothermal system and temperature) is checked on the phase and shape evolution of the fluoride nanocrystals. It is found that reaction time and temperature of these nanocrystals using EDA (180 °C, 6 h) is lower than those of them using OA (220 °C, 10 h). The photoluminescence properties of these fluorides activated by some rare earth ions (Nd 3+ , Eu 3+ , Tb 3+ ) are studied, and especially up-conversion luminescence of the four fluoride nanocrystal systems (Ba 2 LaF 7 :Yb, Tm(Er), Ba 2 REF 7 :Yb, Tm(Er) (RE = Gd, Y, Lu)) is observed

Thin films nanostructured to multidetection catalytic from rare earth minerals: A) purification of perovskite

International Nuclear Information System (INIS)

Silva, M.G. da; Souza, C.P. de; Gomes, U.U.; Paskocimas, C.A.

2010-01-01

This project aims at the use of Brazilian mineral pretreated with high contents of rare earth (La, Ce) aiming at the elaboration of thin films which have physical properties (optical, electrical and catalytic) scalable. The property of greatest interest is the interaction in terms of selective catalytic gases methane, carbon monoxide and ammonia. The materials were characterized by X-ray diffraction (XRD) and transition electron microscopy (TEM). Crystalline residue samples were subjected to a series of chemical treatments followed by alkaline fusion. From a first approach, it was possible to separate the phosphate and silicate mineral residue, separating the rare earth elements to then extract the oxide phases of these materials as complex mixtures. (author)

High purity neodymium acetate from mixed rare earth carbonates

International Nuclear Information System (INIS)

Queiroz, Carlos A. da Silva; Rocha, Soraya M. Rizzo da; Vasconcellos, Mari E. de; Lobo, Raquel M.; Seneda, Jose A.; Pedreira, Walter dos R.

2011-01-01

A simple and economical chemical process for obtaining high purity neodymium acetate is discussed. The raw material in the form rare earth carbonate is produced industrially from the chemical treatment of Brazilian monazite. Ion exchange chromatography technique with a strong cationic resin, proper to water treatment, and without the use of retention ions was used for the fractionating of the rare earth elements (REE). In this way, it was possible to obtain 99.9% pure Nd 2 O 3 in yields greater than or equal 80%, with the elution of the REE using ammonium salt of ethylenediaminetetraacetic acid (EDTA) solution in pH controlled. The complex of EDTA-neodymium was transformed into neodymium oxide, which was subsequently dissolved in acetic acid to obtain the neodymium acetates. Molecular absorption spectrophotometry was used to monitor the neodymium content during the process and sector field inductively coupled plasma mass spectrometry was used to certify the purity of the neodymium acetates. The typical neodymium acetates obtained contain the followings contaminants in μg g -1 : Sc(5.1); Y (0.9); La (1.0); Ce (6.1); Pr (34,4); Sm (12.8); Eu (1.1); Gd (15.4); Tb (29.3); Dy (5.2), Ho(7.4); Er (14.6); Tm (0.3); Yb (2.5); Lu (1.0). The high purity neodymium acetates obtained from this procedure have been applied, replacing the imported product, in research and development area on rare earth catalysts. (author)

Calcium-borosilicate glass-ceramics wasteforms to immobilize rare-earth oxide wastes from pyro-processing

Energy Technology Data Exchange (ETDEWEB)

Kim, Miae [Department of Materials Science and Engineering and Division of Advanced Nuclear Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Gyeongbuk, 790-784 (Korea, Republic of); Heo, Jong, E-mail: jheo@postech.ac.kr [Department of Materials Science and Engineering and Division of Advanced Nuclear Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Gyeongbuk, 790-784 (Korea, Republic of); Department of Materials Engineering, Adama Science and Technology University (ASTU), PO Box 1888, Adama (Ethiopia)

2015-12-15

Glass-ceramics containing calcium neodymium(cerium) oxide silicate [Ca{sub 2}Nd{sub 8-x}Ce{sub x}(SiO{sub 4}){sub 6}O{sub 2}] crystals were fabricated for the immobilization of radioactive wastes that contain large portions of rare-earth ions. Controlled crystallization of alkali borosilicate glasses by heating at T ≥ 750 °C for 3 h formed hexagonal Ca–silicate crystals. Maximum lanthanide oxide waste loading was >26.8 wt.%. Ce and Nd ions were highly partitioned inside Ca–silicate crystals compared to the glass matrix; the rare-earth wastes are efficiently immobilized inside the crystalline phases. The concentrations of Ce and Nd ions released in a material characterization center-type 1 test were below the detection limit (0.1 ppb) of inductively coupled plasma mass spectroscopy. Normalized release values performed by a product consistency test were 2.64·10{sup −6} g m{sup −2} for Ce ion and 2.19·10{sup −6} g m{sup −2} for Nd ion. Results suggest that glass-ceramics containing calcium neodymium(cerium) silicate crystals are good candidate wasteforms for immobilization of lanthanide wastes generated by pyro-processing. - Highlights: • Glass-ceramic wasteforms containing Ca{sub 2}Nd{sub 8-x}Ce{sub x}(SiO{sub 4}){sub 6}O{sub 2} crystals were synthesized to immobilize lanthanide wastes. • Maximum lanthanide oxide waste loading was >26.8 wt.%. • Ce and Nd ions were highly partitioned inside Ca–Nd–silicate crystals compared to glass matrix. • Amounts of Ce and Nd ions released in the material characterization center-type 1 were below the detection limit (0.1 ppb). • Normalized release values performed by a PCT were 2.64• 10{sup −6} g m{sup −2} for Ce ions and 2.19• 10{sup −6} g m{sup −2} for Nd ions.

The operator technique in the theory of the rare earth ion interaction with ligand nuclei

International Nuclear Information System (INIS)

Anikeenok, O.A.; Eremin, M.V.; Khutsishvili, O.G.

1986-01-01

The tensor structure of the operator of rare earth ion interaction with nuclei of close ligands conditioned by virtual processes of charge transport is established. It is taken into account that virtual processes of electron transport from the ligand can take place to the non-filled 4f-, void 5d- and 6s- and preliminarily excited 5p-shells of the rare earth ion. Effects of 4f- and 5d-state mixing by the odd crystal field are considered for the first time. In contrast to the usual multipole-dipole interaction the given one is characterized by anomalously greater significance of highest multipole momenta of the rare earth ion and in the common case it does not have axial symmetry. The theory is compared with data on double electron-nuclear resonance and radiofrequency discrete saturation, taking CaF 2 :Ce 3+ impurity centers as an example

Melting temperature and structural transformation of some rare-earth metals

International Nuclear Information System (INIS)

Vu Van Hung; Hoang Van Tich; Dang Thanh Hai

2009-01-01

the pressure dependence of the melting temperatures of rare-earth metals is studied using the equation of states derived from the statistical moment (SMM). SMM studies were carried out order to calculate the Helmholtz free energy of hcp, bcc Dy and fcc, bcc Ce metals at a wide range of temperatures. the stable phase of Dy and Ce metals can be determined by examining the Helmholtz free energy at a given temperature, i, e. the phase that gives the lowest free energy will be stable. For example, we found that at T lower than 1750 K the hcp Dy metal is stable. At T higher than 1750 K the bcc Dy metal is also stable. Thus 1750 K marks the phase transition temperature of Dy metal. These findings are in agreement with previous experiments. (author)

Rare-earth elements in uranium deposits in the municipality of Pedra, Pernambuco, Brazil

International Nuclear Information System (INIS)

Kennedy Francys Rodrigues Damascena; Romilton dos Santos Amaral; Jose Araujo dos Santos Junior; Alberto Antonio da Silva; Romulo Simoes Cezar Menezes

2015-01-01

In the present study, soil and rock samples were collected from uranium deposits in the city of Pedra, Pernambuco, Brazil. These samples were analyzed using neutron activation analysis to identify the occurrence of rare-earth elements (REE). The most abundant elements found were Ce, Nd and La, with concentrations 12 times higher than the average in the earth's crust and 4.6 times higher than values reported in worldwide studies, including Brazil. Nonetheless, further studies to examine the economic feasibility of mining REEs from this site are necessary. (author)

Recovering heavy rare earth metals from magnet scrap

Science.gov (United States)

Ott, Ryan T.; McCallum, Ralph W.; Jones, Lawrence L.

2017-08-08

A method of treating rare earth metal-bearing permanent magnet scrap, waste or other material in a manner to recover the heavy rare earth metal content separately from the light rare earth metal content. The heavy rare earth metal content can be recovered either as a heavy rare earth metal-enriched iron based alloy or as a heavy rare earth metal based alloy.

Synergism between rare earth cerium(IV) ion and vanillin on the corrosion of cold rolled steel in 1.0 M HCl solution

Energy Technology Data Exchange (ETDEWEB)

Li Xianghong [Department of Fundamental Courses, Southwest Forestry University, Kunming 650224 (China)], E-mail: xianghong-li@163.com; Deng Shuduan [Department of Wood Science and Technology, Southwest Forestry University, Kunming 650224 (China); Fu Hui [Department of Fundamental Courses, Southwest Forestry University, Kunming 650224 (China); Mu Guannan [Department of Chemistry, Yunnan University, Kunming 650091 (China)

2008-12-15

The synergism between rare earth cerium(IV) ion and vanillin on the corrosion of cold rolled steel (CRS) in 1.0 M HCl solution was first investigated by weight loss, potentiodynamic polarization, ultraviolet and visible spectrophotometer (UV-vis), X-ray photoelectron spectroscopy (XPS) and atomic force microscope (AFM). The results revealed that vanillin had a moderate inhibitive effect, and the adsorption of vanillin obeyed the Temkin adsorption isotherm. For rare earth Ce{sup 4+}, it had a negligible effect. However, incorporation of Ce{sup 4+} with vanillin significantly improved the inhibition performance, and produced strong synergistic inhibition effect. Depending on the results, the synergism mechanism was proposed.

Synergism between rare earth cerium(IV) ion and vanillin on the corrosion of cold rolled steel in 1.0 M HCl solution

International Nuclear Information System (INIS)

Li Xianghong; Deng Shuduan; Fu Hui; Mu Guannan

2008-01-01

The synergism between rare earth cerium(IV) ion and vanillin on the corrosion of cold rolled steel (CRS) in 1.0 M HCl solution was first investigated by weight loss, potentiodynamic polarization, ultraviolet and visible spectrophotometer (UV-vis), X-ray photoelectron spectroscopy (XPS) and atomic force microscope (AFM). The results revealed that vanillin had a moderate inhibitive effect, and the adsorption of vanillin obeyed the Temkin adsorption isotherm. For rare earth Ce 4+ , it had a negligible effect. However, incorporation of Ce 4+ with vanillin significantly improved the inhibition performance, and produced strong synergistic inhibition effect. Depending on the results, the synergism mechanism was proposed

A major light rare-earth element (LREE) resource in the Khanneshin carbonatite complex, southern Afghanistan

Science.gov (United States)

Tucker, Robert D.; Belkin, Harvey E.; Schulz, Klaus J.; Peters, Stephen G.; Horton, Forrest; Buttleman, Kim; Scott, Emily R.

2012-01-01

The rapid rise in world demand for the rare-earth elements (REEs) has expanded the search for new REE resources. We document two types of light rare-earth element (LREE)-enriched rocks in the Khanneshin carbonatite complex of southern Afghanistan: type 1 concordant seams of khanneshite-(Ce), synchysite-(Ce), and parisite-(Ce) within banded barite-strontianite alvikite, and type 2 igneous dikes of coarse-grained carbonatite, enriched in fluorine or phosphorus, containing idiomorphic crystals of khanneshite-(Ce) or carbocernaite. Type 1 mineralized barite-strontianite alvikite averages 22.25 wt % BaO, 4.27 wt % SrO, and 3.25 wt % ∑ LREE2O3 (sum of La, Ce, Pr, and Nd oxides). Type 2 igneous dikes average 14.51 wt % BaO, 5.96 wt % SrO, and 3.77 wt % ∑ LREE2O3. A magmatic origin is clearly indicated for the type 2 LREE-enriched dikes, and type 1 LREE mineralization probably formed in the presence of LREE-rich hydrothermal fluid. Both types of LREE mineralization may be penecontemporaneous, having formed in a carbonate-rich magma in the marginal zone of the central vent, highly charged with volatile constituents (i.e., CO2, F, P2O5), and strongly enriched in Ba, Sr, and the LREE. Based on several assumptions, and employing simple geometry for the zone of LREE enrichment, we estimate that at least 1.29 Mt (million metric tonnes) of LREE2O3 is present in this part of the Khanneshin carbonatite complex.

Selective extraction and recovery of rare earth metals from phosphor powders in waste fluorescent lamps using an ionic liquid system.

Science.gov (United States)

Yang, Fan; Kubota, Fukiko; Baba, Yuzo; Kamiya, Noriho; Goto, Masahiro

2013-06-15

The recycling of rare earth metals from phosphor powders in waste fluorescent lamps by solvent extraction using ionic liquids was studied. Acid leaching of rare earth metals from the waste phosphor powder was examined first. Yttrium (Y) and europium (Eu) dissolved readily in the acid solution; however, the leaching of other rare earth metals required substantial energy input. Ionization of target rare earth metals from the waste phosphor powders into the leach solution was critical for their successful recovery. As a high temperature was required for the complete leaching of all rare earth metals, ionic liquids, for which vapor pressure is negligible, were used as an alternative extracting phase to the conventional organic diluent. An extractant, N, N-dioctyldiglycol amic acid (DODGAA), which was recently developed, showed a high affinity for rare earth metal ions in liquid-liquid extraction although a conventional commercial phosphonic extractant did not. An effective recovery of the rare earth metals, Y, Eu, La and Ce, from the metal impurities, Fe, Al and Zn, was achieved from the acidic leach solution of phosphor powders using an ionic liquid containing DODGAA as novel extractant system. Copyright © 2013 Elsevier B.V. All rights reserved.

Influence of rare earth oxides in the oxidation of chromia forming alloys

International Nuclear Information System (INIS)

Ramanathan, L.V.

1989-01-01

The influence of superficial application of rare earth oxides such as CeO sub(2), La sub(2)O sub(3), Nd sub(2)O sub(3), Sm sub(2)O sub(3), and Gd sub(2)O sub (3) to AISI 304 and 310 stainless steels, on their isothermal oxidation behavior at 900 sup(0) and 1000 sup(0)C, and cyclic oxidation behavior between 20 sup(0) and 1000 sup(0)C has been studied. The application of rare earth oxides (REO) has been found to increase the oxidation resistance at AISI 304. No significant improvements in oxidation resistance of AISI 310 were noted. The oxidation resistance of AISI 304 was highest in the presence of CeO sub(2) on its surface. The other REO in decreasing order of influence on oxidation resistance are La sub(2)O sub(3), Nd sub(2)O sub(3), Sm sub(2)O sub(3) and Gd sub(2)O sub(3). SEM investigations of the oxide scale morphology revealed that the improved resistance is probably due to the formation of a thin layer of fine grained compact Cr sub(2)O sub(3) and the higher adhesion of the scale to its increased plasticity. (author)

Quantum efficiency of silica-coated rare-earth doped yttrium silicate

International Nuclear Information System (INIS)

Cervantes-Vásquez, D.; Contreras, O.E.; Hirata, G.A.

2013-01-01

The photoluminescent properties of rare earth-activated white-emitting Y 2 SiO 5 :Ce,Tb nanocrystalline phosphor prepared by two different methods, pressure-assisted combustion synthesis and sol–gel, were studied. The synthesized phosphor samples were post-annealed at 1373 K and 1623 K in order to obtain the X1-Y 2 SiO 5 and X2-Y 2 SiO 5 phases, respectively, which were confirmed by X-ray diffraction measurements. Photoluminescence analysis showed the contribution of two blue-emission bands within the 380–450 nm region originating from 5d–4f transitions in Ce 3+ ions and a well-defined green emission of Tb 3+ ions located at 545 nm corresponding to 5 D 4 → 7 F 5 electronic transitions. Thereafter, Y 2 SiO 5 :Ce,Tb powders were coated with colloidal silica in order to investigate the effect of silica coatings on their luminescent properties. Absolute fluorescence quantum efficiency measurements were carefully performed, which revealed an increase of 12% of efficiency in coated compared with bare-Y 2 SiO 5 :Ce,Tb phosphor. -- Highlights: • Y 2 SiO 5 :Ce,Tb phosphor powders were successfully coated with colloidal silica. • Post-annealing treatments improved the quantum efficiency of silica-coated Y 2 SiO 5 :Ce,Tb phosphors. • Absolute fluorescence quantum efficiency measurements showed an increase of 12%

High-resolution nonresonant x-ray Raman scattering study on rare earth phosphate nanoparticles

NARCIS (Netherlands)

Huotari, Simo; Suljoti, Edlira; Sahle, Christoph J.; Raedel, Stephanie; Monaco, Giulio; de Groot, Frank M. F.

2015-01-01

We report high-resolution x-ray Raman scattering studies of high-order multipole spectra of rare earth 4d -> 4f excitations (the N-4,N-5 absorption edge) in nanoparticles of the phosphates LaPO4, CePO4, PrPO4, and NdPO4. We also present corresponding data for La 5p -> 5d excitations (the O-2,O-3

Structure study and properties of rare earth-rich glassed for the conditioning of nuclear waste

International Nuclear Information System (INIS)

Bardez, I.

2004-11-01

A new nuclear glass composition, able to immobilize highly radioactive liquid wastes from high burn-up UO 2 fuel, was established and its structure studied. The composition of the selected rare earth-rich glass is (molar %): 61.79 SiO 2 - 8.94 B 2 O 3 - 3.05 Al 2 O 3 - 14.41 Na 2 O - 6.32 CaO - 1.89 ZrO 2 - 3.60 RE 2 O 3 (with RE = La, Ce, Pr and Nd) The aim of this study was to determine the local environment of the rare earth in this glass and also to glean information about the effect of glass composition on the rare earth neighbouring (influence of Si, B, Al, Na and Ca contents). To this end, several series of glasses, prepared from the baseline glass, were studied by different characterisation methods such as EXAFS spectroscopy at the neodymium L III -edge, optical absorption spectroscopy, Raman spectroscopy and 29 Si, 27 Al and 11 B MAS-NMR. By coupling all the results obtained, several hypotheses about the nature of the rare earth neighbouring in the glass were proposed. (author)

Sintered cobalt-rare earth intermetallic product

International Nuclear Information System (INIS)

Benz, M.C.

1975-01-01

A process is described for preparing novel sintered cobalt--rare earth intermetallic products which can be magnetized to form permanent magnets having stable improved magnetic properties. A cobalt--rare earth metal alloy is formed having a composition which at sintering temperature falls outside the composition covered by the single Co 5 R intermetallic phase on the rare earth richer side. The alloy contains a major amount of the Co 5 R intermetallic phase and a second solid CoR phase which is richer in rare earth metal content than the Co 5 R phase. The specific cobalt and rare earth metal content of the alloy is substantially the same as that desired in the sintered product. The alloy, in particulate form, is pressed into compacts and sintered to the desired density. The sintered product is comprised of a major amount of the Co 5 R solid intermetallic phase and up to about 35 percent of the product of the second solid CoR intermetallic phase which is richer in rare earth metal content than the Co 5 R phase

Influence of rare earth additions on the oxidation resistance of chromia forming alloys; Influencia da adicao de terras raras sobre a resistencia a oxidacao de ligas formadoras de cromia

Energy Technology Data Exchange (ETDEWEB)

Pillis, Marina Fuser

1995-12-31

The addition of rare earths to alloys, either in elemental form or as surface coatings reduces the oxidation rate of chromia forming alloys. The rare earths either act as nucleation sites for surface oxides or get incorporates into the surface oxide and diffuse to oxide grain boundaries. If the latter occurs, a change in the defect structure close to the grain boundaries, probably takes place. In this manner, the rare earths inhibits the movement of chromium ions to the oxide/gas interface. The influence of rare earth additions to AISI 316, AISI 316L and Ni-20 Cr on their oxidation behavior has been studied., AISI 316+Ce, AISI 316+Y, Ni-20 Cr and Ni-20 Cr-2 Al-1 Ce were prepared by melting and AISI 316L, AISI 316L+Ce O{sub 2} and AISI 316L+Y{sub 2} O{sub 3} by powder compaction. The effect of superficial deposits of rare earth oxides was also studied. The alloys were coated with rare earth oxides by high temperature conversion of the respective rare earth nitrates. Isothermal oxidation tests were carried out at 900-1100 deg C and the cyclic oxidation tests consisted of 6 cycles of 2 hours each at 900 deg C, followed by cooling to room temperature. All the tests were carried out in air. Oxidation behavior was evaluated gravimetrically. Scanning electron microscopy was used to study surface morphology. Energy dispersive analysis and X-ray diffraction techniques were used to identify oxide constituents. Overall, it has been observed that with the addition of rare earths, oxidation resistance increases by decreasing oxidation rates and increasing oxide adhesion. Addition of rare earths to AISI 316 prepared by melting resulted in rapid formation of a chromium rich oxide layered near the metal/oxide interface which reduced overall oxidation rate. The addition of Ce O{sub 2} to AISI 316L was found to improve oxidation behavior after 10 hours at 1100 deg C and also inhibit the formation of volatile Cr O{sub 3}. The isothermal oxidation behavior of rare earth oxide covered

HfO2 - rare earth oxide systems in the region with high content of rare earth oxide

International Nuclear Information System (INIS)

Shevchenko, A.V.; Lopato, L.M.

1982-01-01

Using the methods of annealing and hardenings (10 2 -10 4 deg/s cooling rate) and differential thermal analysis elements of state diagrams of HfO 2 - rare earth oxide (rare earths-La, Pr, Nd, Sm, Gd, Tb, Dy, Y, Er, Yb, Lu, Sc) systems from 1800 deg C up to melting in the range of 60-100 mol% rare earth oxide concentration were constructed. Regularities of HfQ 2 addition effect on high-temperature polymorphic transformations of rare earth oxides were studied. Results of investigation were discussed from viewpoint of crystal chemistry

Production of rare earth-silicon-iron alloys

International Nuclear Information System (INIS)

Mehra, O.K.; Bose, D.K.; Gupta, C.K.

1987-01-01

At Metallurgy Division, BARC, improved procedures for producing rare earth-silicon alloys have been investigated. In these methods, reduction of mixed rare earth oxide by a ferro-silicon and aluminium mixture in combination with CaO-MgO flux/CaO-CaF 2 flux have been tried to prepare an alloy product with a higher rare earth recovery at a higher rare earth content than the present commercial production method. The rare earth recovery using CaO-CaF 2 was 85 per cent while in the case of CaO-MgO flux it was 76 per cent. The corresponding rare earth contents in the alloy correspond to 40 per cent and 55 per cent by weight respectively. (author)

Rare earth metals-primary resources and prospects of processing secondary resources in India

International Nuclear Information System (INIS)

Pandey, B.D.

2015-01-01

) select rare earths (Y, Ce, Eu, La, Tb, Sm, Co, etc) from a few secondary resources, is described in brief. (author)

Rare earth mobility in hydrothermal ore-forming systems

International Nuclear Information System (INIS)

Cornell, D.H.; Schade, J.; Scheepers, R.; Watkeys, M.K.

1988-01-01

Rocks and ores which form by magmatic processes display a range of chondrite-normalised rare earth profiles. One REE (rare earth elements) profile feature which seems unrelated to magmatic processes is the birdwing profile, in which both heavy and light rare earths are enriched relative to the middle rare earths. Birdwing rare earth profiles are an easily identified geochemical anomaly. It is proposed that rare earth geochemistry could be applied in geochemical prospecting for ore formed by hydrothermal processes. 5 figs

Extraction of rare earth elements with organophosphorus extractants as carriers in supported liquid membranes

International Nuclear Information System (INIS)

Kopunec, R.; Benitez, J.C.

1991-01-01

The membrane extraction of Y, Ce, Eu, Tm and their binary mixtures Ce-Y, Ce-Eu, Ce-Tm with supported liquid membranes containing TBP and HDEHP as carriers in decane-dodecane hydrocarbon solvent, has been studied. Upon extraction with TBP aqueous nitrate solutions of rare earth elements (REE) were used as feed phase. In some cases they also contained EDTA or DCTA. In most cases, the receiving phase was an aqueous solution of EDTA. Extraction with HDEHP was performed from nitrate and chloride solutions and the receiving phase was the corresponding dilute acid. Pertraction of an element through a membrane was studied as a function of time and of initial composition of phases. The results are presented in the following forms: flux of metal through membrane, coefficients of permeability, separation factors and effective diffusion coefficients. (author) 24 refs.; 8 figs.; 3 tabs

Distribution of rare earth elements in an alluvial aquifer affected by acid mine drainage: the Guadiamar aquifer (SW Spain)

International Nuclear Information System (INIS)

Olias, M.; Ceron, J.C.; Fernandez, I.; Rosa, J. de la

2005-01-01

This work analyses the spatial distribution, the origin, and the shale-normalised fractionation patterns of the rare earth elements (REE) in the alluvial aquifer of the Guadiamar River (south-western Spain). This river received notoriety in April 1998 for a spill that spread a great amount of slurry (mainly pyrites) and acid waters in a narrow strip along the river course. Groundwaters and surface waters were sampled to analyse, among other elements, the REEs. Their spatial distribution shows a peak close to the mining region, in an area with low values of pH and high concentrations of sulphates and other metals such as Zn, Cu, Co, Ni, Pb, and Cd. The patterns of shale-normalised fractionation at the most-contaminated points show an enrichment in the middle rare earth elements (MREE) with respect to the light (LREE) and heavy (HREE) ones, typical of acid waters. The Ce-anomaly becomes more negative as pH increases, due to the preferential fractionation of Ce in oxyhydroxides of Fe. - Pollution of the aquifer with rare earth elements is documented at a site of a major spill from a mining operation

The Rare Earth Magnet Industry and Rare Earth Price in China

Directory of Open Access Journals (Sweden)

Ding Kaihong

2014-07-01

Full Text Available In the past four years, the price of rare earth metal fluctuates sharply for many reasons. Currently, it has become more stable and more reasonable. This presentation is focused on the effect about the rare earth metal price. Some motor manufacturers have shifted from rare earth permanent magnet to ferrite magnet. Many motor manufacturers changed the design for the motor cooling system to make the motor function at a lower temperature. Thus the consumption of Dy can be markedly reduced. As for manufacturer of NdFeB magnet, we are also trying to optimize our process to reduce to dependence of HREE such as Dy and Tb. HS process have been introduced to solve the problem. With more and more people focusing and engaging on the REE industry, the price of REE will be more transparent without too many fluctuations. China is considering the problems of balancing the environment, energy sources, and labor sources. The application field about NdFeB such as wind turbine generator, HEV/EV, FA /OA is flourishing.

The Rare Earth Magnet Industry and Rare Earth Price in China

Science.gov (United States)

Ding, Kaihong

2014-07-01

In the past four years, the price of rare earth metal fluctuates sharply for many reasons. Currently, it has become more stable and more reasonable. This presentation is focused on the effect about the rare earth metal price. Some motor manufacturers have shifted from rare earth permanent magnet to ferrite magnet. Many motor manufacturers changed the design for the motor cooling system to make the motor function at a lower temperature. Thus the consumption of Dy can be markedly reduced. As for manufacturer of NdFeB magnet, we are also trying to optimize our process to reduce to dependence of HREE such as Dy and Tb. HS process have been introduced to solve the problem. With more and more people focusing and engaging on the REE industry, the price of REE will be more transparent without too many fluctuations. China is considering the problems of balancing the environment, energy sources, and labor sources. The application field about NdFeB such as wind turbine generator, HEV/EV, FA /OA is flourishing.

Application and evaluation of the mass spectrometric isotope dilution technique in the determination of rare earths in geological materials

International Nuclear Information System (INIS)

Moraes, N.M.P. de.

1988-01-01

Establishment of the experimental procedures employed in the rare earth element determination of geological samples by mass spectrometric isotope dilution analysis is discussed in the present work. The procedures involve preparation and calibration of the isotope tracers isotope dilution, dissolution in a teflon pressure vessel, chemical separation and isotope analysis using a fully automated Micromass VG ISOTOPES model 354 thermal ionization mass spectrometer. For the initial chemical separation of total rare earths the cationic resin was employed and HC1 and HNO 3 acids as eluents. In the second step rare earths elements were separated into individual (La, Ce and Nd) and subgroups (Sm-Eu-Gd, Yb-Er-Dy) fractions using the same cationic resin and α-HIBA as eluent. Nine elements La, Ce, Nd, Sm, Eu, Gd, Dy, Er and Yb are determined by this method in the ''United States Geological Survey'' (USGS) standard samples GSP-1, AGV-1 and G-2, with an overall precision of +- 1 to 2% and an accuracy of 5%. The concentration of rare earth element determined in the standard sample PCC-1 showed that the total analytical blanks are in submicrogram levels. The concentration of rare earth elements in the same USGS standard samples were also determined by Instrumental neutron activation analysis, neutron activation analysis with chemical separation before irradiation and inductively coupled argon plasma spectroscopy. The chemical procedures employed for these methods are the same as that used for mass spectrometric isotope dilution. Based on the results obtained, each method was evaluated pointing out their merits and defects. The study clearly showed that the chemical procedure employed for all these techniques was satisfactory. (author) [pt

Rare earth elements behavior in Peruibe black mud

International Nuclear Information System (INIS)

Torrecilha, Jefferson K.; Carvalho, Leandro P.; Gouvea, Paulo F.M.; Silva, Paulo S.C. da

2015-01-01

Rare earth elements in sediments have been used as powerful tools for environmental studies because of their behavior during geochemical processes and are also widely accepted as reliable provenance tracers because they are largely water-immobile and thus behave conservatively during sedimentary processes. The Peruibe Black Mud (PBM) is a sedimentary deposit originated from the interactions of marine sediments and organic matter in an estuarine environment that originates a peloid currently used for medicinal purposes. The objective of this study was to examine rare earth elements pattern distribution in the Peruibe black mud sedimentary deposit as a proxy for its geochemical development. Elemental ratios such as LaN/YbN, Th/U and La/Th were determined and a normalization of the mean rare earth elements concentrations in the samples related to NASC indicates that the light (La to Eu) rare earth elements present values close to the unity while the heavy (Tb to Lu) rare earth elements are depleted related to NASC. It can be observed that the light rare earth elements present enrichment values slightly enriched over the unity while the heavy rare earth elements present values generally below the unity reflecting the enrichment of the light rare earth elements over the heavy rare earth. Rare earth elements concentrations determined in Peruibe black mud samples showed a distribution similar to that found in the NASC for the light rare earth elements and depleted for the heavy rare earth elements. (author)

Rare earth elements behavior in Peruibe black mud

Energy Technology Data Exchange (ETDEWEB)

Torrecilha, Jefferson K.; Carvalho, Leandro P.; Gouvea, Paulo F.M.; Silva, Paulo S.C. da, E-mail: jeffkoy@usp.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2015-07-01

Rare earth elements in sediments have been used as powerful tools for environmental studies because of their behavior during geochemical processes and are also widely accepted as reliable provenance tracers because they are largely water-immobile and thus behave conservatively during sedimentary processes. The Peruibe Black Mud (PBM) is a sedimentary deposit originated from the interactions of marine sediments and organic matter in an estuarine environment that originates a peloid currently used for medicinal purposes. The objective of this study was to examine rare earth elements pattern distribution in the Peruibe black mud sedimentary deposit as a proxy for its geochemical development. Elemental ratios such as LaN/YbN, Th/U and La/Th were determined and a normalization of the mean rare earth elements concentrations in the samples related to NASC indicates that the light (La to Eu) rare earth elements present values close to the unity while the heavy (Tb to Lu) rare earth elements are depleted related to NASC. It can be observed that the light rare earth elements present enrichment values slightly enriched over the unity while the heavy rare earth elements present values generally below the unity reflecting the enrichment of the light rare earth elements over the heavy rare earth. Rare earth elements concentrations determined in Peruibe black mud samples showed a distribution similar to that found in the NASC for the light rare earth elements and depleted for the heavy rare earth elements. (author)

Evidence of Coulomb correction and spinorbit coupling in rare-earth dioxides CeO 2, PrO 2 and TbO 2: An ab initio study

KAUST Repository

Kanoun, Mohammed; Reshak, A. H.; Kanoun-Bouayed, Nawel; Goumri-Said, Souraya

2012-01-01

The current study investigates the structural, elastic, electronic and optical properties of CeO 2, PrO 2 and TbO 2 using the full potential (linearized) augmented plane wave plus local orbital method within the WuCohen generalized gradient approximation (GGA) with Hubbard (U) correction and spinorbit coupling (SOC). The GGAU implementation lead us to describe correctly the relativistic effect on 4f electrons for CeO 2. We clarify that the inclusion of the Hubbard U parameter and the spinorbit coupling are responsible for the ferromagnetic insulating of PrO 2 and TbO 2. The magnetic description is achieved by the spin-density contours and magnetic moment calculations, where we show the polarization of oxygen atoms from the rare earth atoms. The mechanical stability is shown via the elastic constants calculations. The optical properties, namely the dielectric function and the reflectivity are calculated for radiation up to 12 eV, giving interesting optoelectronic properties to these dioxides. © 2011 Elsevier B.V. All rights reserved.

Evidence of Coulomb correction and spinorbit coupling in rare-earth dioxides CeO 2, PrO 2 and TbO 2: An ab initio study

KAUST Repository

Kanoun, Mohammed

2012-04-01

The current study investigates the structural, elastic, electronic and optical properties of CeO 2, PrO 2 and TbO 2 using the full potential (linearized) augmented plane wave plus local orbital method within the WuCohen generalized gradient approximation (GGA) with Hubbard (U) correction and spinorbit coupling (SOC). The GGAU implementation lead us to describe correctly the relativistic effect on 4f electrons for CeO 2. We clarify that the inclusion of the Hubbard U parameter and the spinorbit coupling are responsible for the ferromagnetic insulating of PrO 2 and TbO 2. The magnetic description is achieved by the spin-density contours and magnetic moment calculations, where we show the polarization of oxygen atoms from the rare earth atoms. The mechanical stability is shown via the elastic constants calculations. The optical properties, namely the dielectric function and the reflectivity are calculated for radiation up to 12 eV, giving interesting optoelectronic properties to these dioxides. © 2011 Elsevier B.V. All rights reserved.

Study of CeO{sub x}, PrO{sub x}, and Ce{sub x}Pr{sub 1-x}O{sub 2-{delta}} films on Si(111) by means of high-energetic X-ray photoelectron spectroscopy; Untersuchung von CeO{sub x}-, PrO{sub x}- und Ce{sub x}Pr{sub 1-x}O{sub 2-{delta}}- Filmen auf Si (111) mittels hochenergetischer Roentgen-Photoelektronenspektroskopie

Energy Technology Data Exchange (ETDEWEB)

Allahgholi, Aschkan

2013-03-15

The intention of this work is to shed light on two much discussed topics in the study of rare earth oxides (REO) by hard x-ray photoelectron spectroscopy (HAXPES): (i) Due to the complex spectral shape of the Ce3d region, there have been many discussions on proper approaches to determine the concentration of Ce{sup 3+} and Ce{sup 4+} species in CeO{sub x} over the last decades. (ii) Recently, the true electron structure of rare earth oxides gained new attention, since ab initio calculations showed the necessity of considering additional inter atomic charge transfer to Ce5d levels. Using HAXPES and resonant HAXPES, the question of the true electronic structure of rare earth oxides is approached from the experimental side. As a third topic, the obtained results for cerium oxide and praseodymium oxide are applied in order to investigate the plasma oxidized mixed oxide Ce{sub x}Pr{sub 1-x}O{sub 2-{delta}} grown on Si(111) during thermal reduction. (orig.)

Sc, Y, La-Lu - Rare Earth Elements

International Nuclear Information System (INIS)

Anon.

1987-01-01

At present extensive efforts are being made in completing work on system number Rare Earth Elements. Part A is devoted to the occurrence of these elements on the earth and in the universe. Part B deals with the pure metals; the 7 volumes published cover the description of the separation from the raw materials, the preparation of pure metals,their uses and toxicology, the physical properties of nuclei, atoms, molecules, and isotopes; in addition the behavior of ions in solution and the electrochemical behavior of rare earth elements are described. The compounds are described in Part C. Part D with 6 volumes has been devoted to the description of coordination compounds and is completed. The volume ''Rare Earth Elements C 10'' deals with the rare earth tellurides, oxide tellurides, tellurates, telluride halides, tellurate halides, sulfide tellurides, selenide tellurides, and alkali rare earth tellurates. Another topic of this volume are the compounds of the rare earth elements with polonium. So far as meaningful and in accordance with all earlier volumes of ''Rare Earth Elements'' Series C, comparative data are presented in sections preceding treatment of the individual compounds and systems

Magnetic properties of RT2Zn20; R = rare earth, T = Fe, Co, Ru, Rh, Os and Ir

International Nuclear Information System (INIS)

Jia, Shuang

2008-01-01

It is well known that rare earth intermetallic compounds have versatile, magnetic properties associated with the 4f electrons: a local moment associated with the Hund's rule ground state is formed in general, but a strongly correlated, hybridized state may also appear for specific 4f electronic configuration (eg. for rare earth elements such as Ce or Yb). On the other hand, the conduction electrons in rare earth intermetallic compounds, certainly ones associated with non hybridizing rare earths, usually manifest non-magnetic behavior and can be treated as a normal, non-interacted Fermi liquid, except for some 3d-transition metal rich binary or ternary systems which often manifest strong, itinerant, d electron dominant magnetic behavior. Of particular interest are examples in which the band filling of the conduction electrons puts the system in the vicinity of a Stoner transition: such systems, characterized as nearly or weakly ferromagnet, manifest strongly correlated electronic properties (Moriya, 1985). For rare earth intermetallic compounds, such systems provide an additional versatility and allow for the study of the behaviors of local moments and hybridized moments which are associated with 4f electron in a correlated conduction electron background.

Preparation of Pt Ru/C + rare earths by the method of reduction by alcohol for the electro-oxidation of ethanol

International Nuclear Information System (INIS)

Tusi, M.M.; Rodrigues, R.M.S.; Spinace, E.V.; Oliveira Neto, A.

2010-01-01

PtRu/C electrocatalyst was prepared in a single step, while that PtRu/85%C-15%Ce, PtRu/85%C-15%La, PtRu/85%C-15%Nd and PtRu/85%C-15%Er electrocatalyst were prepared in a two step. In the first step a Carbon Vulcan XC72 + rare earth supports were prepared. In the second step PtRu electrocatalyst were prepared by an alcohol-reduction process using ethylene glycol as solvent and reducing agent and supported on Vulcan XC72 + earth rare. The obtained electrocatalysts were characterized by EDAX, XRD and chronoamperometry. The electro-oxidation of ethanol was studied by chronoamperometry at room temperature. PtRu/85%C- 15%Ce electrocatalyst showed a significant increase of performance for ethanol oxidation compared to PtRu/C electrocatalyst. (author)

Rare Earth Metals: Resourcefulness and Recovery

Science.gov (United States)

Wang, Shijie

2013-10-01

When we appreciate the digital revolution carried over from the twentieth century with mobile communication and the Internet, and when we enjoy our high-tech lifestyle filled with iDevices, hybrid cars, wind turbines, and solar cells in this new century, we should also appreciate that all of these advanced products depend on rare earth metals to function. Although there are only 136,000 tons of annual worldwide demand, (Cho, Rare Earth Metals, Will We Have Enough?)1 rare earth metals are becoming such hot commodities on international markets, due to not only to their increasing uses, including in most critical military hardware, but also to Chinese growth, which accounts for 95% of global rare earth metal production. Hence, the 2013 technical calendar topic, planned by the TMS/Hydrometallurgy and Electrometallurgy Committee, is particularly relevant, with four articles (including this commentary) contributed to the JOM October Issue discussing rare earth metals' resourcefulness and recovery.

Electric and magnetic properties of oxidic titanium bronzes of rare earths Lnsub(2/3+x)TiOsub(3+-y) with perovskite structure

International Nuclear Information System (INIS)

Bazuev, G.V.; Makarova, O.V.; Shvejkin, G.P.

1983-01-01

A study was made on electric and magnetic properties of oxidic titanium bronzes of rare earths and their dependence on rare earth nature and the degree of rare earth sublattice filling was followed. Data on Lnsub(2/3)TiOsub(3-y) (Ln-Ce, Nd) anion-deficient perovskites are given as well. Investigated Cesub(2/3)TiOsub(2.985) and Ndsub(2/3)TiOsub(2.875) phases as well as defectless with respect to oxygen Lnsub(2/3)TiOsub(3) phases have rhombic structure of perovskite type with ordered position of Ln 3 + cations and vacancies. Specific electric resistance and thermoelectromotive force factor were determined in vacuum at 290-1173 K for samples in the form of parallelepiped of 3x5x25 mm 3 size. Magnetic susceptibility chi was determined at 77-300 K by Faraday method using a device based on magnetic balancewith electromagnetic compensation. Relative error during chi measuring didn't exceed +-2%. Collectivized behaviour of d-electrons of Ti 3 + cations in oxidic titanium bronzes of rare earths: Lnsub(2/3+x)TiOsub(3+-y) (Ln-La, Ce, Nd; 0 < x < 1/3), conditioned by formation of narrow, partly filled π*-zone, was established on the basis of measuring specific electric resistance and magnetic susceptibility

Microstructure and fatigue behaviors of a biomedical Ti–Nb–Ta–Zr alloy with trace CeO2 additions

International Nuclear Information System (INIS)

Song, Xiu; Wang, Lei; Niinomi, Mitsuo; Nakai, Masaaki; Liu, Yang; Zhu, Miaoyong

2014-01-01

The new β-type Ti–29Nb–13Ta–4.6Zr (TNTZ) alloy containing trace amounts of CeO 2 additions has been designed as a biomedical implant with improved fatigue properties achieved by keeping Young's modulus to a low value. The results show that the microstructure is refined by the addition of CeO 2 ; the β grain size becomes a little larger when Ce content increases from 0.05% to 0.10%. This occurs because dispersed CeO 2 particles can act as nucleation sites for β grains; thus, the effect of rare earth oxides on microstructure refinement mainly depends on the size and dispersion of the rare earth oxides. Young's moduli of TNTZ with CeO 2 additions are maintained as low as those of TNTZ without CeO 2 , while the fatigue limit is highly improved. The 0.10% Ce alloy exhibits the best fatigue strength among the experimental alloys; its fatigue strength is increased by 66.7% compared to that of pure TNTZ. The mechanism by which rare earth oxides affect fatigue performance is dominated by dispersion strengthening. The stiff rare earth oxides can hinder the movement of dislocations, resulting in resistance to the formation of fatigue cracks. Rare earth oxides also change the crack propagation direction and the crack propagation route, effectively decreasing the crack propagation rate

Selective extraction and recovery of rare earth metals from phosphor powders in waste fluorescent lamps using an ionic liquid system

International Nuclear Information System (INIS)

Yang, Fan; Kubota, Fukiko; Baba, Yuzo; Kamiya, Noriho; Goto, Masahiro

2013-01-01

Highlights: • Recycling of rare earth metals from fluorescent lamps was conducted by ionic liquid-mediated extraction. • Acid leaching from a waste phosphor powder was carried out using sulfuric and nitric acids. • An ionic liquid was used as extracting solvent for the rare earth metals. • Selective extraction of rare earth metals from leach solutions was attained. •The extracting ionic liquid phase was recyclable in the recovery process. -- Abstract: The recycling of rare earth metals from phosphor powders in waste fluorescent lamps by solvent extraction using ionic liquids was studied. Acid leaching of rare earth metals from the waste phosphor powder was examined first. Yttrium (Y) and europium (Eu) dissolved readily in the acid solution; however, the leaching of other rare earth metals required substantial energy input. Ionization of target rare earth metals from the waste phosphor powders into the leach solution was critical for their successful recovery. As a high temperature was required for the complete leaching of all rare earth metals, ionic liquids, for which vapor pressure is negligible, were used as an alternative extracting phase to the conventional organic diluent. An extractant, N, N-dioctyldiglycol amic acid (DODGAA), which was recently developed, showed a high affinity for rare earth metal ions in liquid–liquid extraction although a conventional commercial phosphonic extractant did not. An effective recovery of the rare earth metals, Y, Eu, La and Ce, from the metal impurities, Fe, Al and Zn, was achieved from the acidic leach solution of phosphor powders using an ionic liquid containing DODGAA as novel extractant system

Selective extraction and recovery of rare earth metals from phosphor powders in waste fluorescent lamps using an ionic liquid system

Energy Technology Data Exchange (ETDEWEB)

Yang, Fan; Kubota, Fukiko; Baba, Yuzo [Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395 (Japan); Kamiya, Noriho [Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395 (Japan); Center for Future Chemistry, Kyushu University, 744 Motooka, Fukuoka 819-0395 (Japan); Goto, Masahiro, E-mail: m-goto@mail.cstm.kyushu-u.ac.jp [Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395 (Japan); Center for Future Chemistry, Kyushu University, 744 Motooka, Fukuoka 819-0395 (Japan)

2013-06-15

Highlights: • Recycling of rare earth metals from fluorescent lamps was conducted by ionic liquid-mediated extraction. • Acid leaching from a waste phosphor powder was carried out using sulfuric and nitric acids. • An ionic liquid was used as extracting solvent for the rare earth metals. • Selective extraction of rare earth metals from leach solutions was attained. •The extracting ionic liquid phase was recyclable in the recovery process. -- Abstract: The recycling of rare earth metals from phosphor powders in waste fluorescent lamps by solvent extraction using ionic liquids was studied. Acid leaching of rare earth metals from the waste phosphor powder was examined first. Yttrium (Y) and europium (Eu) dissolved readily in the acid solution; however, the leaching of other rare earth metals required substantial energy input. Ionization of target rare earth metals from the waste phosphor powders into the leach solution was critical for their successful recovery. As a high temperature was required for the complete leaching of all rare earth metals, ionic liquids, for which vapor pressure is negligible, were used as an alternative extracting phase to the conventional organic diluent. An extractant, N, N-dioctyldiglycol amic acid (DODGAA), which was recently developed, showed a high affinity for rare earth metal ions in liquid–liquid extraction although a conventional commercial phosphonic extractant did not. An effective recovery of the rare earth metals, Y, Eu, La and Ce, from the metal impurities, Fe, Al and Zn, was achieved from the acidic leach solution of phosphor powders using an ionic liquid containing DODGAA as novel extractant system.

Structure, electronic properties, luminescence and chromaticity investigations of rare earth doped KMgBO{sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Zheng, Jianghui; Cheng, Qijin [School of Energy Research, Xiamen University, Xiamen 361005 (China); Wu, Shunqing [Department of Physics, Xiamen University, Xiamen, 361005 (China); Zhuang, Yixi [College of Materials, Xiamen University, Xiamen 361005 (China); Guo, Ziquan; Lu, Yijun [Department of Electronic Science, Fujian Engineering Research Center for Solid-state Lighting, Xiamen University, Xiamen 361005 (China); Chen, Chao, E-mail: cchen@xmu.edu.cn [School of Energy Research, Xiamen University, Xiamen 361005 (China); Department of Physics, Xiamen University, Xiamen, 361005 (China); Department of Electronic Science, Fujian Engineering Research Center for Solid-state Lighting, Xiamen University, Xiamen 361005 (China)

2015-09-01

In this work, the optimization of the geometry and the electronic properties of the host matrix KMgBO{sub 3} were investigated using density functional theory, and the comprehensive photoluminescence and chromaticity properties on five rare earth ion-doped (RE = Ce{sup 3+}, Tm{sup 3+}, Tb{sup 3+}, Eu{sup 3+}, Dy{sup 3+}) KMgBO{sub 3} phosphors were also studied. By introducing RE ions into the KMgBO{sub 3} host, excellent purple, blue, green, red and white emitting light could be obtained under the near-ultraviolet light excitation. The results suggest that rare earth doped KMgBO{sub 3} phosphors are potential luminescence materials for the application in the near-ultraviolet white light-emitting diodes. - Highlights: • The electronic properties of the host matrix KMgBO{sub 3} were investigated. • The PL properties on rare earth ions doped KMgBO{sub 3} phosphors were studied. • The chromaticity properties on rare earth ions doped KMgBO{sub 3} samples were studied. • Tm{sup 3+} and Eu{sup 3+} doped KMgBO{sub 3} samples show higher color purity than commercial phosphors.

Trace rare earth analysis by neutron activation and γ-ray/x-ray spectrometry

International Nuclear Information System (INIS)

Laul, J.C.; Nielson, K.K.; Wogman, N.A.

1977-01-01

A rare earth group separation scheme followed by photon energy analysis using Ge(Li) and intrinsic Ge detectors enhances significantly the detection of individual rare earth elements (REE) at or below the ppb level. Based on the x-ray and selected γ-ray energies, Ge(Li) γ-ray counting is favorable for 140 La, 141 Ce, 142 Pr, 153 Sm, 171 Er, and 177 Lu, whereas intrinsic Ge γ-ray counting is favorable for 143 Ce, 147 Nd, 160 Tb, and 166 Ho, and intrinsic Ge x-ray counting is favorable for 152 Eu and 175 Yb. Gamma-ray counting of 153 Gd and 170 Tm is equally sensitive with Ge(Li) or intrinsic Ge detectors. Precise measurements of the REE were made in the USGS geological samples BCR-1, W-1, AGV-1, G2, GSP-1 and PCC-1, the IAEA Soil-5, and the NBS orchard leaf and bovine liver standards. Their chondritic normalized REE patterns behave as a smooth function of the REE ionic radii. Interestingly, the REE patterns observed in orchard leaf and other plants are identical to the REE pattern in bovine liver. This comparison leads us to suggest that the plant REE patterns are probably not further fractionated by animals such as bovine during their dietary plant uptake

Preparation of rare earth fluorides from apatite concentrate

International Nuclear Information System (INIS)

Mulyarchuk, I.F.; Voloshchenko, M.V.; Zen'kovich, E.G.; Sumenkova, V.V.; AN Ukrainskoj SSR, Kiev. Inst. Problem Lit'ya)

1980-01-01

The processes of preparation of the rare earths element sum from apatite concentrate of the Khibins, connected with preliminary extraction of rare earth phosphates from nitric acid extract using solvent extraction or direct precipitation from the extract by solution of potassium and ammonium fluorides. The sequence of the processes of the first variant is the following: solvent extraction of rare earths by tributylphosphate from clarified nitric acid extract of apatite with subsequent reextraction of rare earths with water and precipitation of rare earth phosphates from aqueous solution during neutralization by ammonia. In case of fluoride preparation from rare earth phosphate the main attention is paid to precipitation and filtration of fluorides. Technological scheme and cost price of industry for the production of 1800 t of rare earth trifluorides a year are calculated. When taking account of TBP losses according to its solubility the industry cost price is 1O times lower the modern cost of rare earth fluorides

Effect of rare earth substitution in cobalt ferrite bulk materials

International Nuclear Information System (INIS)

Bulai, G.; Diamandescu, L.; Dumitru, I.; Gurlui, S.; Feder, M.; Caltun, O.F.

2015-01-01

The study was focused on the influence of small amounts of rare earth (RE=La, Ce, Sm, Gd, Dy, Ho, Er, Yb) addition on the microstructure, phase content and magnetic properties of cobalt ferrite bulk materials. The X-Ray diffraction measurements confirmed the formation of the spinel structure but also the presence of secondary phases of RE oxides or orthoferrite in small percentages (up to 3%). Density measurements obtained by Archimedes method revealed a ~1 g cm −3 decrease for the RE doped cobalt ferrite samples compared with stoichiometric one. Both the Mössbauer and Fourier Transform Infrared Spectrocopy analysis results confirmed the formation of the spinel phase. The saturation magnetization and coercive field values of the doped samples obtained by Vibrating Sample Magnetometry were close to those of the pure cobalt ferrite. For magnetostrictive property studies the samples were analyzed using the strain gauge method. Higher maximum magnetostriction coefficients were found for the Ho, Ce, Sm and Yb doped cobalt ferrite bulk materials as related to the stoichiometric CoFe 2 O 4 sample. Moreover, improved strain derivative was observed for these samples but at higher magnetic fields due to the low increase of the coercive field values for doped samples. - Highlights: • Substitution by a large number of rare earth elements was investigated. • First reported results on magnetostriction measurements of RE doped cobalt ferrite. • The doped samples presented an increased porosity and a decreased grain size. • Increased magnetostrctive response was observed for several doped samples

RE{sub 2}B{sub 8}O{sub 15} (RE = La, Pr, Nd). Syntheses of three new rare earth borates isotypic to Ce{sub 2}B{sub 8}O{sub 15}

Energy Technology Data Exchange (ETDEWEB)

Glaetzle, Matthias; Hoerder, Gregor J.; Huppertz, Hubert [Innsbruck Univ. (Austria). Inst. fuer Allgemeine, Anorganische und Theoretische Chemie

2016-08-01

The rare earth borates RE{sub 2}B{sub 8}O{sub 15} (RE = La, Pr, Nd) were synthesized in a Walker-type multianvil apparatus under conditions of 5.5 GPa and 1100 C. Starting from the corresponding rare earth oxides and boron oxide, the syntheses yielded crystalline products of all new compounds that allowed crystal structure analyses based on single-crystal X-ray diffraction data for La{sub 2}B{sub 8}O{sub 15} and Nd{sub 2}B{sub 8}O{sub 15}. The compound Pr{sub 2}B{sub 8}O{sub 15} could be characterized via X-ray powder diffractometry. The results show that the new compounds crystallize isotypically to Ce{sub 2}B{sub 8}O{sub 15} in the monoclinic space group P2/c. The infrared spectra of RE{sub 2}B{sub 8}O{sub 15} (RE = La, Pr, Nd) have also been studied.

Thermochemistry of rare-earth trifluorides

International Nuclear Information System (INIS)

Kim, K.Y.; Johnson, C.E.

1981-01-01

Using the most recent crystallographic data, the Born-Lande equation was employed to calculate lattice energies of the rare-earth trifluorides. The excellent agreement ( 0 sub(f)(MX 3 ,c,298.15K) can be estimated. The magnitude of the monotonic change of ΔH 0 sub(f)(MX 3 ) for the rare-earth trihalides series (14 4f electrons) is comparable to the energy change between Sc and Ti in which only one 3d electron is added. This energy change is consistent with the chemical evidence that the electrons in the f-orbitals of rare earths contribute negligibly to the bonding. (author)

Pressure dependence of magnetic ordering temperatures of rare earth-Sn/sub 3/ compounds

Energy Technology Data Exchange (ETDEWEB)

Foner, S [Massachusetts Inst. of Tech., Cambridge (USA). Francis Bitter National Magnet Lab.

1979-12-01

Measurements of the hydrostatic pressure dependence of the Neel temperatures, Tsub(N), are reported for PrSn/sub 3/, NdSn/sub 3/, GdSn/sub 3/ and CeIn/sub 3/. Tsub(N) is found to increase with applied pressure for PrSn/sub 3/ and NdSn/sub 3/, whereas Tsub(N) is pressure independent within experimental error for GdSn/sub 3/ and CeIn/sub 3/. Slightly Sn-deficient RESn/sub 3/ (RE = rare earth) compounds are found consistently to be weakly ferromagnetic. The physical properties of the RESn/sub 3/ compounds exhibit analogies with the corresponding properties of dilute superconducting (LaRE)Sn/sub 3/ alloys. The high pressure data for PrSn/sub 3/ and CeIn/sub 3/ are qualitatively consistent with a 'Kondo necklace' model for magnetically ordered RE compounds with unstable 4f shells.

Pressure dependence of magnetic ordering temperatures of rare earth - Sn/sub 3/ compounds

Energy Technology Data Exchange (ETDEWEB)

DeLong, L E [Virginia Univ., Charlottesville (USA). Dept. of Physics; Guertin, R P; Foner, S

1979-12-01

Measurements of the hydrostatic pressure dependence of the Neel temperatures, Tsub(N), are reported for PrSn/sub 3/, NdSn/sub 3/, GdSn/sub 3/ and CeIn/sub 3/. Tsub(N) is found to increase with applied pressure for PrSn/sub 3/ and NdSn/sub 3/, whereas Tsub(N) is pressure independent within experimental error for GdSn/sub 3/ and CeIn/sub 3/. Slightly Sn-deficient RESn/sub 3/ (RE=rare earth) compounds are found consistently to be weakly ferromagnetic. The physical properties of the RESn/sub 3/ compounds exhibit analogies with the corresponding properties of dilute superconducting (LaRE)Sn/sub 3/ alloys. The high pressure data for PrSn/sub 3/ and CeIn/sub 3/ are qualitatively consistent with a 'Kondo necklace' model for magnetically ordered RE compounds with unstable 4f shells.

Rare earth elements as a tool for studying the formation of cemented layers in an area affected by acid mine drainage

International Nuclear Information System (INIS)

Grawunder, Anja; Lonschinski, Martin; Merten, Dirk; Büchel, Georg

2015-01-01

Highlights: • Spatially resolved analysis of 14 rare earth elements (REE) by LA-ICP-MS. • Positive correlation of Mn contents and (positive) Ce anomalies. • Linkage of the two cemented layer’s formation to soil solution and groundwater. - Abstract: In a profile with two cemented layers sampled in an area affected by acid mine drainage, both have rare earth element (REE) signatures with positive Ce anomalies in the Post Archean Australian Shale-normalised patterns. Both cemented layers have higher contents of environmentally relevant metals (Cd, Co, Cu, Fe, Mn, U, and Zn) than the over- and underlying unconsolidated Quaternary sediments and are depleted of Al, Ca, K, and Mg. The cemented layers are enriched in middle and heavy REE, but only the bulk pattern of the lower cemented layer reveals a positive Ce anomaly. For the upper cemented layer, this positive Ce anomaly was only determined by spatially resolved laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) studies only for segments with a high abundance of Mn, occurring as Mn phases as proven by energy dispersive X-ray spectroscopy. The Mn phases are formed secondarily to the ferric cement and are especially enriched in Ce and Co. The Ce anomaly of the lower cemented layer most probably is inherited from groundwater to the ferric cement, whereas the Ce anomaly of the upper cemented layer is the result of preferential scavenging of Ce onto the Mn phases compared to other REE

Development of constraint algorithm for the number of electrons in molecular orbitals consisting mainly 4f atomic orbitals of rare-earth elements and its introduction to tight-binding quantum chemical molecular dynamics method

International Nuclear Information System (INIS)

Endou, Akira; Onuma, Hiroaki; Jung, Sun-ho

2007-01-01

Our original tight-binding quantum chemical molecular dynamics code, Colors', has been successfully applied to the theoretical investigation of complex materials including rare-earth elements, e.g., metal catalysts supported on a CeO 2 surface. To expand our code so as to obtain a good convergence for the electronic structure of a calculation system including a rare-earth element, we developed a novel algorithm to provide a constraint condition for the number of electrons occupying the selected molecular orbitals that mainly consist of 4f atomic orbitals of the rare-earth element. This novel algorithm was introduced in Colors. Using Colors, we succeeded in obtaining the classified electronic configurations of the 4f atomic orbitals of Ce 4+ and reduced Ce ions in a CeO 2 bulk model with one oxygen defect, which makes it difficult to obtain a good convergence using a conventional first-principles quantum chemical calculation code. (author)

Choice of excitation source for determination of rare earth elements with radioisotope excited X ray fluorescence

International Nuclear Information System (INIS)

Zhang Quanshi; Chang Yongfu

2000-01-01

The comparisons of two radioisotope source ( 241 Am and 238 Pu) which are the most available in the radioisotope excited X Ray Fluorescence (XRF) analysis technique and two characteristic X ray series (KX and LX) analyzed for the determination of the rare-earth (RE) elements were investigated in detail. According to the principle of emission and detection of X ray , the relative excitation efficiencies were calculated by the some fundamental physical parameters including the photoelectric mass attenuation coefficient, the fluorescent yield, the absorption jump factor, the emission probability of the detected fluorescent line with reference to other liens of the same series etc., The advantages and disadvantages of the two conditions are discussed. These results may determine the optimal excitation and detection conditions for different rare-earth elements. The experimental results with nine rare-earth elements (Ce, Nd, Sm, Tb, Tm, Ho, Er, Yb and Lu) are in agreement with the results of theoretical calculations

Rare Earth Polyoxometalates.

Science.gov (United States)

Boskovic, Colette

2017-09-19

Longstanding and important applications make use of the chemical and physical properties of both rare earth metals and polyoxometalates of early transition metals. The catalytic, optical, and magnetic features of rare earth metal ions are well-known, as are the reversible multielectron redox and photoredox capabilities of polyoxomolybdates and polyoxotungstates. The combination of rare earth ions and polyoxometalates in discrete molecules and coordination polymers is of interest for the unique combination of chemical and physical properties that can arise. This Account surveys our efforts to synthesize and investigate compounds with rare earth ions and polyoxometalates (RE-POMs), sometimes with carboxylate-based organic coligands. Our general synthetic approach is "bottom-up", which affords well-defined nanoscale molecules, typically in crystalline form and amenable to single-crystal X-ray diffraction for structure determination. Our particular focus is on elucidation of the physical properties conferred by the different structural components with a view to ultimately being able to tune these properties chemically. For this purpose, we employ a variety of spectroscopic, magnetochemical, electrochemical, and scattering techniques in concert with theoretical modeling and computation. Studies of RE-POM single-molecule magnets (SMMs) have utilized magnetic susceptibility, inelastic neutron scattering, and ab initio calculations. These investigations have allowed characterization of the crystal field splitting of the rare earth(III) ions that is responsible for the SMM properties of slow magnetic relaxation and magnetization quantum tunneling. Such SMMs are promising for applications in quantum computing and molecular spintronics. Photophysical measurements of a family of hybrid RE-POMs with organic ligands have afforded insights into sensitization of Tb(III) and Eu(III) emission through both organic and polyoxometalate chromophores in the same molecule. Detailed

Extraction and separation of Am and rare earth elements in HNO3 solution with P507-sulphonating kerosene

International Nuclear Information System (INIS)

Li Zhenhu; Jiao Rongzhou; Zhu Yongjun

1994-01-01

A study has been made of the extraction equilibrium of Am(III) and rare earth elements (III) in HNO 3 solution with P507-sulphonating kerosene. It has been found that this equilibrium depends on saponification ratio of P507, feed acidity, metal concentration as well as phase ratio. The extraction ability in order is La< Ce< Am< Pr< Nd< Sm. The model of distribution ratio has been founded. The agreement for calculated and experimental values of distribution ratio is fairly good. These values can be used to design the extraction and separation process of Am and rare earth elements

Thermodynamics of rare earths in steelmaking

International Nuclear Information System (INIS)

Vahed, A.; Kay, D.A.R.

1976-01-01

The standard free energies of formation of the oxides, sulfides and oxysulfides of cerium and lanthanum under steelmaking conditions have been calculated and used to predict the behavior of rare earths in steelmaking. Deoxidation and desulfurization constants, expressed in terms of Henrian activities, have been used to construct a precipitation diagram which indicates the sequence of rare earth inclusion formation. An enrichment of lanthanum in (RE)-oxysulfide and cerium in (RE)-sulfide is predicted. It is also predicted that rare earths should be able to reduce the soluble oxygen and sulfur contents of liquid steel well below the contents presently found in most industrial and laboratory practices. A simple method of calculating steelmaking additions for complete rare earth control of inclusion composition is presented

Effect of Rare Earth Element on Microstructure and Properties of in situ Synthesized TiB2/Al Composites

Directory of Open Access Journals (Sweden)

QU Min

2018-03-01

Full Text Available The effect of rare earth element Ce, Sc and Er on TiB2 particles and matrix alloy micros-tructure of TiB2/Al composites was studied with in situ synthesis method. It shows that the addition of rare earth element improves the microstructure and properties of TiB2/Al composites notably. The particles of TiB2 are relatively homogenously distributed as adding 0.3% (mass fraction rare earth element Sc and Er, moreover, it is Er that refines the microstructure of matrix alloy most significantly, then is Sc. Similarly, it is demonstrated that the addition of Sc and Er results in better tensile strength, which is enhanced by 32% and 31%, respectively; the addition of Er also leads to the best ductility by 85% with optimal tensile property. Meanwhile, fracture morphology analysis reveals that the fracture of the composites is microporous gathered ductile fracture when adding Sc and Er. Finally, it is verified that the mechanism of rare earth element on composites lies in two aspects:one is that the addition of rare earth element improves the wettability of the composites and suppresses the agglomeration of TiB2 particles; the other is that the addition of rare earth element refines the microstructure of matrix alloy and then improves the tensile strength of the composites.

Theory of Rare-Earth Alloys

DEFF Research Database (Denmark)

Lindgård, Per-Anker

1977-01-01

A mean-field random alloy theory combined with a simple calculation of the exchange interaction J(c,Q) is shown to quantitatively account for the phase diagrams for alloys of rare-earth metals with Y, Lu, Sc, and other rare-earth metals. A concentration-dependent J(c,Q) explains the empirical 2...

Solvent extraction of rare earths from thiocyanate medium using N,N,N',N'-tetra-2-ethylhexyl diglycolamide

International Nuclear Information System (INIS)

Anitha, M.; Kotekar, M.K.; Singh, D.K.; Sharma, J.N.; Singh, H.

2014-01-01

TEHDGA (N,N,N',N'-tetra-2-ethylhexyl diglycolamide), a neutral extractant, has been explored for separation of Yttrium from other heavy rare earths (Er) from thiocyanate medium. Presence of 5%(v/v) isodecyl alcohol was found to be optimum to prevent third phase formation. Experimental variables such as TEHDGA concentration (0.05M-0.2M), thiocyanate concentration (0.01M-0.04M), aqueous pH, rare earth concentration (0.25g/L-5g/L), temperature (35℃-65℃), stripping reagents on extraction of rare earths were investigated. The extraction of rare earths increased with increase in TEHDGA concentration and the dependency of distribution ratio of rare earth on TEHDGA concentrations is shown. The slopes were analysed to be approximately 3 for all the rare earths. The effect of thiocyanate concentration on distribution ratio is depicted. Based on slope analysis technique, the extracted species was found to be RE(SCN) 3 .3TEHDGA. The distribution ratio values decreased, may possibly be due to decrease in free extractant concentration in the organic phase, from 8.4 to 0.1 for Y with increase in yttrium concentration in the range of 0.25g/L to 5g/L. The extraction of rare earth decreased with increase in temperature indicating exothermic in nature and the enthalpy change (ΔH) obtained for Y(III) was -14.27KJ/mol. Among stripping reagents studied, oxalic acid was efficient in quantitative stripping of rare earths from TEHDGA. The extraction efficiency for rare earths by TEHDGA increased with increase in atomic number: La< Ce< Pr< Nd< Sm< Y< Eu< Gd< Tb< Dy< Ho< Er< Tm< Lu irrespective of thiocyanate concentration. Separation factors between these metal ions were also evaluated. High separation factor of 6.4 for Er/Y pair at 0.03M thiocyanate has indicated the feasibility of using TEHDGA as extractant to separate Y from Er and other rare earths as an alternative for Aliquat 336-thiocyanate system developed in our laboratory

Study of polyoxide catalysts of methane combustion on Mn, Cu, Ni, rare earth elements, alkaline earth elements base by the X-ray fluorescence analysis method

International Nuclear Information System (INIS)

Grigor'eva, V.P.; Popova, N.M.; Zheksenbaeva, Z.T.; Sass, A.S.; Salakhova, R.Kh.; Dosumov, K.D.

2002-01-01

The results of X-ray fluorescence analysis of polyoxide catalysts on of Mn, Cu, Ni, rare earth elements, alkaline earth elements base supported on 2 % Ce/θ-Al 2 O 3 are presented. This polyoxide catalysts are using for deep methane oxidation. DRON-4-7 X-ray diffractometers was applied for the analysis. It was found, that oxides in Ni-Cu-Cr catalysts after long time heating up to 1200 deg. C have been interacted with catalyst supports with Ni(Cu)Al 2 O 3 aluminates formation and due to its decomposition transformation degree of CH 4 to CO 2 are reduced. Activity of MnBaSrCeLa catalysts after heating up to 1200 deg. C does not changed

Determination of Rare Earth Elements in Geological Samples Using Laser-Induced Breakdown Spectroscopy (LIBS).

Science.gov (United States)

Bhatt, Chet R; Jain, Jinesh C; Goueguel, Christian L; McIntyre, Dustin L; Singh, Jagdish P

2018-01-01

Laser-induced breakdown spectroscopy (LIBS) was used to detect rare earth elements (REEs) in natural geological samples. Low and high intensity emission lines of Ce, La, Nd, Y, Pr, Sm, Eu, Gd, and Dy were identified in the spectra recorded from the samples to claim the presence of these REEs. Multivariate analysis was executed by developing partial least squares regression (PLS-R) models for the quantification of Ce, La, and Nd. Analysis of unknown samples indicated that the prediction results of these samples were found comparable to those obtained by inductively coupled plasma mass spectrometry analysis. Data support that LIBS has potential to quantify REEs in geological minerals/ores.

Rare earth element geochemistry of South Atlantic deep sea sediments: Ce anomaly change at approx. 54 My

International Nuclear Information System (INIS)

Wang, Y.L.; Liu, Y.-G.; Schmitt, R.A.; Oregon State Univ., Corvallis; Oregon State Univ., Corvallis; Oregon State Univ., Corvallis

1986-01-01

The geochemistry of the REE (rare earth elements) in oceanic sediments is discussed, based mainly on samples from DSDP Holes 530A and 530B, Leg 75, and Hole 525A, Leg 74. The proposed mechanisms for incorporation of the REE into the marine carbonate phases are adsorption, chiefly onto the carbonate minerals and on Sc, Hf, and Ta-rich FE-Mn hydroxide flocs as carbonate coatings. The Ce anomaly of marine carbonate was used as an indicator of paleo-ocean water redox conditions: the bottom water of the Angola Basin was in a reducing condition in the Cretaceous. At ca. 54 My, the South Atlantic water condition became oxidizing, similar to the present seawater redox condition. This change was related to the improvement of circulation due to the widening of South Atlantic and the subsidence of water circulation barriers such as the Walvis Ridge and perhaps the Romanche Fracture Zone. The REE abundances and patterns of younger sediments in the Angola Basin (YSAB) are very similar to those observed in NASC, PAAS, and ES sediments. The YSAB REE abundances and patterns may represent the average REE distribution of the exposed African continental crust. The strong resemblance of REE distributions of YSAB, NASC, PAAS and ES suggests thorough REE mixing from different sources and the uniformity of the average crustal compositions of different continents: Africa, North America, Australia, and Europe. (author)

Using Ce to modify inclusion in spring steel

Directory of Open Access Journals (Sweden)

Wang Q.

2017-01-01

Full Text Available The effect of rare earth metals addition on the Al2O3 inclusions in spring steel used in fastener of high speed railway was investigated by metallographic examination, SEM-EDS and composition analysis. To deform those harmful inclusions to improve material performance，the evolution process of Al2O3 inclusions was investigated through the surface and line scanning. Ce metal modifying Al2O3 is a stepwise reduction process based on a formation of ring shape Ce-riched band around the Al2O3 inclusions during reaction process. Through experiment and thermodynamic calculation, an evolvement rule about Al2O3 inclusions change after Ce addition is obtained, i.e. Al2O3→Ce2O3-Al2O3→Ce2O2S. Changing the inclusions from Al2O3 to rare earth inclusions could improve the resistance to pitting corrosion based on potentiodynamic anodic polarization test.

Enhanced pinning in mixed rare earth-123 films

Science.gov (United States)

Driscoll, Judith L [Los Alamos, NM; Foltyn, Stephen R [Los Alamos, NM

2009-06-16

An superconductive article and method of forming such an article is disclosed, the article including a substrate and a layer of a rare earth barium cuprate film upon the substrate, the rare earth barium cuprate film including two or more rare earth metals capable of yielding a superconductive composition where ion size variance between the two or more rare earth metals is characterized as greater than zero and less than about 10.times.10.sup.-4, and the rare earth barium cuprate film including two or more rare earth metals is further characterized as having an enhanced critical current density in comparison to a standard YBa.sub.2Cu.sub.3O.sub.y composition under identical testing conditions.

Rare earths production and marketing opportunities

International Nuclear Information System (INIS)

Falconnet, P.G.

1988-01-01

The rare earths (RE) market is relatively small. The total production during 1968 was only 10000 tons (REO) which rose to 27000 tons (REO) during 1985. The three major areas of application, which are volume market for ceric rare earths are catalysts, glass ceramics and metallurgy. Among the other uses of rare earths, the permanent magnets, lamp phosphors and fine ceramics have registered significant growth in RE consumption. Monazite and bastnasite are the main natural source for rare earths and processing of these for one of the rare earths in high demand leads to over production of some others not in demand, thus creating a balance problem. The growth in RE market has always been influenced by the technology shifts and product substitution. For example, the RE consumption during 1974/76 for desulfurization of steel had substantially decreased due to the usage of calcium. Similarly, 1985 had witnessed a drastic cut in the use of REs in fluid cracking due to the introduction of stabilized zeolites which contain less REO. Thus, the overall compound growth rate of demand was only 3.9 % per year during the period 1970-1985. At present, 37 % of the rare earths production goes to the glass/ceramics industry, 33 % for catalyst and 25 % to metallurgy. The price of REs constantly shows a downward trend. This trend coupled with the rapid changes taking place in the various technological fields, demands greater flexibility and high marketing skills from the RE producers. The key factor for future expansion of RE market will be the development of 'high volume' application of ceric rare earths. (author) 2 figs., 8 tabs

Afganistan and rare earths

Directory of Open Access Journals (Sweden)

Emilian M. Dobrescu

2013-05-01

Full Text Available On our planet, over a quarter of new technologies for the economic production of industrial goods, are using rare earths, which are also called critical minerals and industries that rely on these precious items being worth of an estimated nearly five trillion dollars, or 5 percent of world gross domestic product. In the near future, competition will increase for the control of rare earth minerals embedded in high-tech products. Rare minerals are in the twenty-first century what oil accounted for in the twentieth century and coal in the nineteenth century: the engine of a new industrial revolution. Future energy will be produced increasingly by more sophisticated technological equipment based not just on steel and concrete, but incorporating significant quantities of metals and rare earths. Widespread application of these technologies will result in an exponential increase in demand for such minerals, and what is worrying is that minerals of this type are almost nowhere to be found in Europe and in other industrialized countries in the world, such as U.S. and Japan, but only in some Asian countries, like China and Afghanistan.

Separation method for rare-earths using high-voltage electrophoresis on paper strip; Methode de separation des terres rares par electrophorese a haute tension sur papier - support

Energy Technology Data Exchange (ETDEWEB)

Clarence, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1966-07-01

The equipment includes an electrophoresis set running at 3 000 V and 20 mA. Two cooling plates are used as heat exchanger, and a pneumatic pressure device to insure an uniform pressure on the paper strip laid flat. The mobilities and the separations of the rare earths in lactic, and, {alpha} hydroxy-isobutyric acid solutions are investigated on cellulose acetate strip. Better results are obtained with {alpha} hydroxy-isobutyric acid. The method is rapid and allows a fine fractionation of rare earth elements within less than an hour. A complete separation of a Ce - Pr - Nd - Pm - Eu mixture, and a Y - Tb mixture is obtained. (author) [French] L'equipement comporte un appareil d'electrophorese fonctionnant sous 3000 V a 20 mA. Deux plaques refrigerantes absorbent la chaleur dissipee, et un coussin pneumatique assure une pression uniforme sur le papier support. Les mobilites et les separations des terres rares sont etudiees en milieux lactiques et {alpha} hydroxyisobutyriques sur papier d'acetate de cellulose. De meilleurs resultats sont obtenus avec l'acide {alpha} hydroxyisobutyrique. La methode est tres rapide et permet de separer un melange de terres rares radioactives en moins d'une heure. Des separations fines d'un melange Ce, Pr, Nd, Pm, Eu, et d'un melange Y, Tb sont egalement obtenues. (auteur)

Processing of monazite at the rare earth division,Udyogamandal

International Nuclear Information System (INIS)

Narayanan, N.S.; Thulasidoss, S.; Ramachandran, T.V.; Swaminathan, T.V.; Prasad, K.R.

1988-01-01

The processing techniques adopted at the Rare Earth Division of the Indian Rare Earths Limited at Udyogamandal, for the production of rare earth compounds of various compositions and purity grades are reviewed. Over 100 different compounds are produced and marketed, and these include mixed rare earths chloride, crude thorium concentrate, cerium oxide, cerium hydrate, rare earths carbonate, didymium salts and individual rare earth oxides and salts. Also, the trisodium phosphate obtained as byproduct in the processing of monazite, is recovered and marketed. The process scheme for monazite essentially involves alkaline digestion of ground monazite, removal of the by-product trisodium phosphate, separation of thorium through preferential dissolution of rare earths hydroxide in hydrochloric acid under controlled pH and temperature conditions followed by purification, and evaporation of the chloride solution to yield pure rare earths chloride. Part of the chloride is utilised for the production of individual rare earth compounds after separation by solvent extraction and ion exchange processes. Individual rare earth compounds of 99.99 %+ purity are regularly produced to cater to the demand within the country. (author) 8 figs., 1 tab

Preparing rare earth-silicon-iron-aluminum alloys

International Nuclear Information System (INIS)

Marchant, J.D.; Morrice, E.; Herve, B.P.; Wong, M.M.

1980-01-01

As part of its mission to assure the maximum recovery and use of the Nation's mineral resources, the Bureau of Mines, investigated an improved procedure for producing rare earth-silicon alloys. For example, a charge consisting of 681 grams of mixed rare-earth oxides, 309 grams of ferrosilicon (75 wt-pct Si), and 182 grams of aluminum metal along with a flux consisting of 681 grams of CaO and 45 grams of MgO was reacted at 1500 0 C in an induction furnace. Good slag-metal separation was achieved. The alloy product contained, in weight-percent, 53 RE, 28 Si, 11 Fe, and 4 Al with a rare earth recovery of 80 pct. In current industrial practice rare earth recoveries are usually about 60 pct in alloy products that contain approximately 30 wt-pct each of rare earths and silicon. Metallurgical evaluations showed the alloys prepared in this investigation to be as effective in controlling the detrimental effect of sulfur in steel and cast iron as the commercial rare earth-silicon-iron alloys presently used in the steel industry

Rare earth element patterns in nigerian coals

International Nuclear Information System (INIS)

Ewa, I.O.B.; Elegba, S.B.

1996-01-01

Rare Earth Elements (REE's) retain group coherence in their environment and are therefore useful geochemical markers. We report the pattern of ten REE's (La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Yb, Lu) determined by Instrumental Neutron Activation Analysis (INAA) for coals obtained from eight mines in Nigeria, namely, Okaba, Enugu, Ogbete, Onyeama, Gombe, Lafia, Asaba and Afikpo. Our results show the existence of fractionations with the highest index of 13.19 for Lafia coal, depletion in HREE, negative Eu anomaly for most of the coals, REE patterns that are consistent with chondritic trends; prominent (Eu/Eu * ) cn for Okaba and Gombe coals. Variations in geochemical data observed could suggest strong departures from band metamorphism during the coalification events of the Benue Trough geosynclines, where the coal deposits are all located. (author) 14 refs., 2 figs., 3 tabs

Double selenates of rare earths and ammonium

International Nuclear Information System (INIS)

Iskhakova, L.D.; Kozlova, N.P.; Makarevich, L.G.

1991-01-01

Double selenates of rare earths with ammonium were prepared in result of crystallization. It is shown that NH 4 Ln(SeO 4 ) · nH 2 O crystalline hydrates are presented by penta-and trihydrates. Existance of two modifications was revealed for NH 4 Ln(SeO 4 ) · 5H 2 O: monoclinic form of NH 4 La(SeO 4 ) 2 · 5H 2 O, isostructural RbCe(SeO 4 ) 2 · 5H 2 O, and earlier unknown rhombic form of salts with Ln = Pr, Nd. Trihydrates with Ln = Sm-Yb belong to structural type of RbNd(SeO 4 ) 2 · 3H 2 O. Anhydrous salts NH 4 Ln(SeO 4 ) 2 are isostructural with monoclinic KNd(SO 4 ) 2 modification. Lattice parameters of binary selenates are presented

Rare Earth Garnet Selective Emitter

Science.gov (United States)

Lowe, Roland A.; Chubb, Donald L.; Farmer, Serene C.; Good, Brian S.

1994-01-01

Thin film Ho-YAG and Er-YAG emitters with a platinum substrate exhibit high spectral emittance in the emission band (epsilon(sub lambda) approx. = 0.75, sup 4)|(sub 15/2) - (sup 4)|(sub 13/2),for Er-YAG and epsilon(sub lambda) approx. = 0.65, (sup 5)|(sub 7) - (sup 5)|(sub 8) for Ho-YAG) at 1500 K. In addition, low out-of-band spectral emittance, epsilon(sub lambda) less than 0.2, suggest these materials would be excellent candidates for high efficiency selective emitters in thermophotovoltaic (TPV) systems operating at moderate temperatures (1200-1500 K). Spectral emittance measurements of the thin films were made (1.2 less than lambda less than 3.0 microns) and compared to the theoretical emittances calculated using measured values of the spectral extinction coefficient. In this paper we present the results for a new class of rare earth ion selective emitters. These emitters are thin sections (less than 1 mm) of yttrium aluminum garnet (YAG) single crystal with a rare earth substitutional impurity. Selective emitters in the near IR are of special interest for thermophotovoltaic (TPV) energy conversion. The most promising solid selective emitters for use in a TPV system are rare earth oxides. Early spectral emittance work on rare earth oxides showed strong emission bands in the infrared (0.9 - 3 microns). However, the emittance outside the emission band was also significant and the efficiency of these emitters was low. Recent improvements in efficiency have been made with emitters fabricated from fine (5 - 10 microns) rare earth oxide fibers similar to the Welsbach mantle used in gas lanterns. However, the rare earth garnet emitters are more rugged than the mantle type emitters. A thin film selective emitter on a low emissivity substrate such as gold, platinum etc., is rugged and easily adapted to a wide variety of thermal sources. The garnet structure and its many subgroups have been successfully used as hosts for rare earth ions, introduced as substitutional

Interactions of rare earth elements with bacteria and organic ligands

International Nuclear Information System (INIS)

Ozaki, Takuo; Suzuki, Yoshinori; Nankawa, Takuya; Yoshida, Takahiro; Ohnuki, Toshihiko; Kimura, Takaumi; Francis, Arokiasamy J.

2006-01-01

We investigated the interactions of rare earth elements (REEs) Eu(III) and/or Ce(III, IV) with the common soil bacterium Pseudomonas fluorescens and organic ligands, such as malic acid, citric acid, a siderophore (DFO), cellulose, chitin, and chitosan. Malic acid formed complexes with Eu(III), but degradation of malic acid was observed when the ratio of malic acid to Eu(III) was higher than 100. Citric acid formed a stoichiometric complex with Eu(III) that was not degraded by P. fluorescens. Adsorption of Eu(III) from the DFO complex occurred as a free ion dissociated from DFO and not as the Eu(III)-DFO complex. Cerium(III) was oxidized to Ce(IV) during complexation with DFO to form the Ce(IV)-DFO complex. Time-resolved laser-induced fluorescence spectroscopy (TRLFS) analysis showed that cellulose, chitin, and chitosan, respectively, formed a weak complex, an inner-spherical complex, and an outer-spherical complex with Eu(III). This method also demonstrated that the coordination environment of Eu(III) adsorbed on P. fluorescens possessed similar characteristics to that of chitin, and revealed that adsorption of Eu(III) on P. fluorescens was through a multidentate and predominantly inner-spherical coordination

Quantum efficiency of silica-coated rare-earth doped yttrium silicate

Energy Technology Data Exchange (ETDEWEB)

Cervantes-Vásquez, D., E-mail: dcervant@cnyn.unam.mx [Centro de Investigación Científica y de Educación Superior de Ensenada, Carretera Ensenada-Tijuana No. 3918, Zona Playitas, C.P. 22860 Ensenada, B.C., México (Mexico); Contreras, O.E.; Hirata, G.A. [Centro de Nanociencias y Nanotecnología, Universidad Nacional Autónoma de México, Km. 107 Carretera Tijuana-Ensenada, C.P. 22800 Ensenada, B.C., México (Mexico)

2013-11-15

The photoluminescent properties of rare earth-activated white-emitting Y{sub 2}SiO{sub 5}:Ce,Tb nanocrystalline phosphor prepared by two different methods, pressure-assisted combustion synthesis and sol–gel, were studied. The synthesized phosphor samples were post-annealed at 1373 K and 1623 K in order to obtain the X1-Y{sub 2}SiO{sub 5} and X2-Y{sub 2}SiO{sub 5} phases, respectively, which were confirmed by X-ray diffraction measurements. Photoluminescence analysis showed the contribution of two blue-emission bands within the 380–450 nm region originating from 5d–4f transitions in Ce{sup 3+} ions and a well-defined green emission of Tb{sup 3+} ions located at 545 nm corresponding to {sup 5}D{sub 4}→{sup 7}F{sub 5} electronic transitions. Thereafter, Y{sub 2}SiO{sub 5}:Ce,Tb powders were coated with colloidal silica in order to investigate the effect of silica coatings on their luminescent properties. Absolute fluorescence quantum efficiency measurements were carefully performed, which revealed an increase of 12% of efficiency in coated compared with bare-Y{sub 2}SiO{sub 5}:Ce,Tb phosphor. -- Highlights: • Y{sub 2}SiO{sub 5}:Ce,Tb phosphor powders were successfully coated with colloidal silica. • Post-annealing treatments improved the quantum efficiency of silica-coated Y{sub 2}SiO{sub 5}:Ce,Tb phosphors. • Absolute fluorescence quantum efficiency measurements showed an increase of 12%.

Electric and magnetic properties of oxidic titanium bronzes of rare earths Lnsub(2/3+x)TiOsub(3+-y) with perovskite structure

Energy Technology Data Exchange (ETDEWEB)

Bazuev, G V; Makarova, O V; Shvejkin, G P [AN SSSR, Sverdlovsk. Inst. Khimii

1983-01-01

A study was made on electric and magnetic properties of oxidic titanium bronzes of rare earths and their dependence on rare earth nature and the degree of rare earth sublattice filling was followed. Data on Lnsub(2/3)TiOsub(3-y) (Ln-Ce, Nd) anion-deficient perovskites are given as well. Investigated Cesub(2/3)TiOsub(2.985) and Ndsub(2/3)TiOsub(2.875) phases as well as defectless with respect to oxygen Lnsub(2/3)TiOsub(3) phases have rhombic structure of perovskite type with ordered position of Ln/sup 3 +/ cations and vacancies. Specific electric resistance and thermoelectromotive force factor were determined in vacuum at 290-1173 K for samples in the form of parallelepiped of 3x5x25 mm/sup 3/ size. Magnetic susceptibility chi was determined at 77-300 K by Faraday method using a device based on magnetic balance with electromagnetic compensation. Relative error during chi measuring didn't exceed +-2%. Collectivized behaviour of d-electrons of Ti/sup 3 +/ cations in oxidic titanium bronzes of rare earths: Lnsub(2/3+x)TiOsub(3+-y) (Ln-La, Ce, Nd; 0 < x < 1/3), conditioned by formation of narrow, partly filled ..pi..*-zone, was established on the basis of measuring specific electric resistance and magnetic susceptibility.

Study on the contents of trace rare earth elements and their distribution in wheat and rice samples by RNAA

International Nuclear Information System (INIS)

Sun Jingxin; Zhao Hang; Wang Yuqi

1994-01-01

The concentrations of 8 REE (La, Ce, Nd, Sm, Eu, Tb, Yb and Lu) in wheat and rice samples have been determined by RNAA. The contents and distributions of REE in each part of the plants (i.e. root, leaf, stem, husk and seed) and their host soils were studied, which included samples applied with rare earth elements in farming and control samples. The effects of applying rare earth on the uptake of REE by the plants and the REE accumulation in the grains of human health were also discussed. (author) 9 refs.; 4 figs.; 4 tabs

Effect of Coulomb interaction on the X-ray magnetic circular dichroism spin sum rule in rare earths

NARCIS (Netherlands)

Teramura, Y; Tanaka, A; Thole, BT; Jo, T

A deviation from the spin sum rule, which relates the integrated intensity of the X-ray magnetic circular dichroism (MCD) signal to the expectation value of the spin operator S-z ((S-z)), is numerically calculated in the case of the 3d --> 4f absorption for rare earths from the trivalent Ce to Tm.

Dissolution of nickel ferrite and rare earths containing magnetites in citric acid - EDTA - gallic acid (CEG) formulation

Energy Technology Data Exchange (ETDEWEB)

Kumbhar, A.G.; Kishore, K.; Venkateswaran, G.; Balaji, V. [Applied Chemistry Div., Bhabha Atomic Research Centre, Mumbai (India)

2002-07-01

It has been shown by us earlier that gallic acid can be used as a reductant in dilute chemical decontaminant formulations containing EDTA as chelant. The results on the dissolution of magnetite in such a formulation were quite promising. Moreover, the superior radiation stability of gallic acid vis-a-vis other reductants such as ascorbic acid or oxalic acid is another plus point for this formulation. Besides having an inherent stability against radiation degradation, it is able to protect even EDTA against radiation induced decomposition to a great extent unlike the case of ascorbic acid. In an extension of that work, dissolution experiments have now been carried out on nickel ferrite and magnetites containing rare earths like La, Ce and Zr This is to simulate the presence of fission product oxides in magnetite resulting from a possible phase of operation with leaky fuel. The rate constants have been determined using the inverse cubic rate law. In the case of nickel ferrite, although there is an initial induction period, the rate constants for the dissolution were determined to be at 1.6 x 10{sup -2} and 3.6 x 10{sup -3} min{sup -1} at 353 K and 333 K respectively. Presence of Ce in particular either alone or in combination with Zr/La at a level of 1 at.% equivalent each in magnetite is seen to increase the surface area of the oxide. The rate constants for the dissolution at 353 K in a 11:44:4 mM CEG formulation taken with magnetite and rare earth containing magnetites equivalent to yielding 22 mM Fe upon complete dissolution are as follows: 5.09 x 10{sup -2} min{sup -1} (magnetite), 7.06 x 10{sup -2} min{sup -1} (Ce{sub 2}O{sub 3} containing magnetite), 6.33 x 10{sup -2} min{sup -1} (Ce{sub 2}O{sub 3}, ZrO{sub 2} containing magnetite), 1 x 10{sup -1} min{sup -1} (Ce{sub 2}O{sub 3}, ZrO{sub 2}, La{sub 2}O{sub 3} containing magnetite). The presence of Ce, Zr and La at 1 at.% level each has not resulted in any turbidity in solution at the end of magnetite dissolution

Dissolution of nickel ferrite and rare earths containing magnetites in citric acid - EDTA - gallic acid (CEG) formulation

International Nuclear Information System (INIS)

Kumbhar, A.G.; Kishore, K.; Venkateswaran, G.; Balaji, V.

2002-01-01

It has been shown by us earlier that gallic acid can be used as a reductant in dilute chemical decontaminant formulations containing EDTA as chelant. The results on the dissolution of magnetite in such a formulation were quite promising. Moreover, the superior radiation stability of gallic acid vis-a-vis other reductants such as ascorbic acid or oxalic acid is another plus point for this formulation. Besides having an inherent stability against radiation degradation, it is able to protect even EDTA against radiation induced decomposition to a great extent unlike the case of ascorbic acid. In an extension of that work, dissolution experiments have now been carried out on nickel ferrite and magnetites containing rare earths like La, Ce and Zr This is to simulate the presence of fission product oxides in magnetite resulting from a possible phase of operation with leaky fuel. The rate constants have been determined using the inverse cubic rate law. In the case of nickel ferrite, although there is an initial induction period, the rate constants for the dissolution were determined to be at 1.6 x 10 -2 and 3.6 x 10 -3 min -1 at 353 K and 333 K respectively. Presence of Ce in particular either alone or in combination with Zr/La at a level of 1 at.% equivalent each in magnetite is seen to increase the surface area of the oxide. The rate constants for the dissolution at 353 K in a 11:44:4 mM CEG formulation taken with magnetite and rare earth containing magnetites equivalent to yielding 22 mM Fe upon complete dissolution are as follows: 5.09 x 10 -2 min -1 (magnetite), 7.06 x 10 -2 min -1 (Ce 2 O 3 containing magnetite), 6.33 x 10 -2 min -1 (Ce 2 O 3 , ZrO 2 containing magnetite), 1 x 10 -1 min -1 (Ce 2 O 3 , ZrO 2 , La 2 O 3 containing magnetite). The presence of Ce, Zr and La at 1 at.% level each has not resulted in any turbidity in solution at the end of magnetite dissolution suggesting chemical dissolution of these rare earth oxides in the formulation. Simple magnetite

NEW RARE EARTH ELEMENT ABUNDANCE DISTRIBUTIONS FOR THE SUN AND FIVE r-PROCESS-RICH VERY METAL-POOR STARS

International Nuclear Information System (INIS)

Sneden, Christopher; Lawler, James E.; Den Hartog, Elizabeth A.; Cowan, John J.; Ivans, Inese I.

2009-01-01

We have derived new abundances of the rare earth elements Pr, Dy, Tm, Yb, and Lu for the solar photosphere and for five very metal-poor, neutron-capture r-process-rich giant stars. The photospheric values for all five elements are in good agreement with meteoritic abundances. For the low-metallicity sample, these abundances have been combined with new Ce abundances from a companion paper, and reconsideration of a few other elements in individual stars, to produce internally consistent Ba, rare earth, and Hf (56 ≤ Z ≤ 72) element distributions. These have been used in a critical comparison between stellar and solar r-process abundance mixes.

Rare earth elements in the Pacific and Atlantic Oceans

International Nuclear Information System (INIS)

Baar, H.J.W. de; Bacon, M.P.; Brewer, P.G.; Bruland, K.W.

1985-01-01

The first profiles of Pr, Tb, Ho, Tm and Lu in the Pacific Ocean, as well as profiles of La, Ce, Nd, Sm, Eu, Gd and Yb are reported. Concentrations of REE (except Ce) in the deep water are two to three times higher than those observed in the deep Atlantic Ocean. Surface water concentrations are typically lower than in the Atlantic Ocean, especially for the heavier elements Ho,Tm,Yb and Lu. Cerium is strongly depleted in the Pacific water column, but less so in the oxygen minimum zone. The distribution of the REE group is consistent with two simultaneous processes: (1) cycling similar to that of opal and calcium carbonate, and (2) adsorptive scavenging by settling particles and possibly by uptake at ocean boundaries. However, the first process can probably not be sustained by the low REE contents of shells, unless additional adsorption on surfaces is invoked. The second process, adsorptive scavenging, largely controls the oceanic distribution and typical seawater pattern of the rare earths. (author)

Alaska's rare earth deposits and resource potential

Science.gov (United States)

Barker, James C.; Van Gosen, Bradley S.

2012-01-01

Alaska’s known mineral endowment includes some of the largest and highest grade deposits of various metals, including gold, copper and zinc. Recently, Alaska has also been active in the worldwide search for sources of rare earth elements (REE) to replace exports now being limitedby China. Driven by limited supply of the rare earths, combined with their increasing use in new ‘green’ energy, lighting, transportation, and many other technological applications, the rare earth metals neodymium, europium and, in particular, the heavy rare earth elements terbium, dysprosium and yttrium are forecast to soon be in critical short supply (U.S. Department of Energy, 2010).

Electrical and dielectric properties of lithium manganate nanomaterials doped with rare-earth elements

Energy Technology Data Exchange (ETDEWEB)

Iqbal, Muhammad Javed; Ahmad, Zahoor [Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan)

2008-05-01

Substituted LiR{sub x}Mn{sub 2} {sub -} {sub x}O{sub 4} (R = La{sup 3+}, Ce{sup 3+}{sub ,} Pr{sup 3+} and x = 0.00 - 0.20) nanoparticles are prepared by the sol-gel method and the consequent changes in their lattice structure, dielectric and electrical parameters are determined by XRD, ED-XRF, SEM, LCR meter bridge and dc electrical resistivity measurements. Diffraction data show that the samples are single-phase spinel materials with crystallites sizes between 21 and 38 nm. The lattice parameter, cell volume and X-ray density are found to be affected by doping the Li-manganate with the rare-earth elements. The ED-XRF analysis confirms the stoichiometric composition of the synthesized samples and SEM reveals their morphology. Calculated values of the dielectric constant ({epsilon}) and the dielectric loss (tan {delta}) decrease with the frequency of the applied field. This is attributed to Maxwell-Wagner polarization. Replacement of manganese by the rare-earth elements results in an improvement in the structural stability of the material, which is considered to be useful for enhancement of the cycleability of the compounds when used in lithium rechargeable batteries, and increases significantly the values of {epsilon} and tan {delta} (except for Ce). Lithium manganate nanomaterials with high {epsilon} and low tan {delta} may be attractive for application in memory storage devices. (author)

Rare earth metal alloy magnets

International Nuclear Information System (INIS)

Harris, I.R.; Evans, J.M.; Nyholm, P.S.

1979-01-01

This invention relates to rare earth metal alloy magnets and to methods for their production. The technique is based on the fact that rare earth metal alloys (for e.g. cerium or yttrium) which have been crumbled to form a powder by hydride formation and decomposition can be used for the fabrication of magnets without the disadvantages inherent in alloy particle size reduction by mechanical milling. (UK)

Metal nitride cluster as a template to tune the electronic and magnetic properties of rare-earth metal containing endohedral fullerenes

International Nuclear Information System (INIS)

Zhang, Yang

2013-01-01

Rare-earth metal containing endohedral fullerenes have attracted much attention due to the feasibility of encaging metal atom, atoms or cluster inside of carbon cages. By switching the metal atom or cluster entrapped inside of the carbon cage the physical and chemical properties of the fullerene compounds can be tuned. The understanding of magnetic and electrochemical properties of endohedral fullerenes plays an essential role in fundamental scientific researches and potential applications in materials science. In this thesis, synthesizing novel rare-earth metal containing endohedral fullerene structures, studying the properties of these isolated endohedral fullerenes and the strategies of tuning the electronic and magnetic properties of endohedral fullerenes were introduced. The DC-arc discharging synthesis of different lanthanide metal-based (Ho, Ce and Pr) mixed metal nitride clusterfullerenes was achieved. Those rare-earth metal containing endohedral fullerenes were isolated by multi-step HPLC. The isolated samples were characterized by spectroscopic techniques included UV-vis-NIR, FTIR, Raman, LDI-TOF mass spectrometry, NMR and electrochemistry. The Ho-based mixed metal nitride clusterfullerenes Ho x M 3-x N rate at C 80 (M= Sc, Lu, Y; x=1, 2) were synthesized by ''reactive gas atmosphere'' method or ''selective organic solid'' route. The isolated samples were characterized by LDI-TOF mass spectrometry, UV-vis-NIR, FTIR, Raman and NMR spectroscopy. The 13 C NMR spectroscopic studies demonstrated exceptional NMR behaviors that resulted from switching the second metal inside of the mixed metal nitride cluster Ho x M 3-x N from Sc to Lu and further to Y. The LnSc 2 N rate at C 80 (Ln= Ce, Pr, Nd, Tb, Dy, Ho, Lu) MMNCFs were characterized by 13 C and 45 Sc NMR study respectively. According to Bleaney's theory and Reilley method, the separation of δ PC and δ con from δ para was achieved by the primary 13 C and 45 Sc NMR analysis of LnSc 2 N rate at C 80 (I). The

Effects of rare earth oxide nanoparticles on root elongation of plants.

Science.gov (United States)

Ma, Yuhui; Kuang, Linglin; He, Xiao; Bai, Wei; Ding, Yayun; Zhang, Zhiyong; Zhao, Yuliang; Chai, Zhifang

2010-01-01

The phytotoxicity of four rare earth oxide nanoparticles, nano-CeO(2), nano-La(2)O(3), nano-Gd(2)O(3) and nano-Yb(2)O(3) on seven higher plant species (radish, rape, tomato, lettuce, wheat, cabbage, and cucumber) were investigated in the present study by means of root elongation experiments. Their effects on root growth varied greatly between different nanoparticles and plant species. A suspension of 2000 mg L(-1) nano-CeO(2) had no effect on the root elongation of six plants, except lettuce. On the contrary, 2000 mg L(-1) suspensions of nano-La(2)O(3), nano-Gd(2)O(3) and nano-Yb(2)O(3) severely inhibited the root elongation of all the seven species. Inhibitory effects of nano-La(2)O(3), nano-Gd(2)O(3), and nano-Yb(2)O(3) also differed in the different growth process of plants. For wheat, the inhibition mainly took place during the seed incubation process, while lettuce and rape were inhibited on both seed soaking and incubation process. The fifty percent inhibitory concentrations (IC(50)) for rape were about 40 mg L(-1) of nano-La(2)O(3), 20mg L(-1) of nano-Gd(2)O(3), and 70 mg L(-1) of nano-Yb(2)O(3), respectively. In the concentration ranges used in this study, the RE(3+) ion released from the nanoparticles had negligible effects on the root elongation. These results are helpful in understanding phytotoxicity of rare earth oxide nanoparticles. Copyright 2009 Elsevier Ltd. All rights reserved.

Preconcentration of rare earth elements from rocks by thin-layer chromatography and their neutron-activation determination

International Nuclear Information System (INIS)

Ryabukhin, V.A.; Volynets, M.P.; Myasoedov, B.F.

1990-01-01

Conditions were studied for separation of rare earths and accompanying elements in rocks on Fixion 50x8 thin-layer plates using solutions of oxalic acid and ammonium chloride in ammonia medium. A simple technique was developed for TLC proconcentration of rare earths followed by gamma spectrometric analysis of the irradiated fractions that enabled to determine 8-10 elements in samples with a mass of up to 30 mg. The limits of detection (μg/g) were 0.05 (Eu), 0.1 (Sm), 0.2 (Tb), 0.3 (Yb), 0.4 (La), 1.0 (Tu), 2.0 (Ce), 10 (Nd). The relative standard deviation was 0.05-0.20 at element levels 5-10 times as high as the detection limits

Determination of Rare Earth Elements in plants by neutron activation analysis

International Nuclear Information System (INIS)

Figueiredo, Ana M.G.; Maria, Sheila P.; Ceccantini, Gregorio C.T.

1996-01-01

In the present work, instrumental neutron activation analysis was employed to the determination of rare earth elements (La, Ce, Nd, Eu, Tb, Yb e Lu) in plants, aiming biogeochemical studies. The precision and accuracy of the method were verified by the analysis of the reference materials Citrus Leaves (NIST 1572) and Pine Needles (NIST 1575). With exception of terbium, the results obtained agreed with reference values, giving relative errors less than 25%. The method was applied to different species of plants growing in the alkaline-ultramafic complex of Salitre, MG and the obtained data were compared to the average content in plants. (author)

Rare earth metals for automotive exhaust catalysts

International Nuclear Information System (INIS)

Shinjoh, Hirohumi

2006-01-01

The usage of rare earth metals for automotive exhaust catalysts is demonstrated in this paper. Rare earth metals have been widely used in automotive catalysts. In particular, three-way catalysts require the use of ceria compounds as oxygen storage materials, and lanthana as both a stabilizer of alumina and a promoter. The application for diesel catalysts is also illustrated. Effects of inclusion of rare earth metals in automotive catalysts are discussed

Rare earths: preparation of spectro chemically pure standards, study of their carbonates and synthesis of a new compound series - the peroxy carbonates

International Nuclear Information System (INIS)

Queiroz, Carlos Alberto da Silva

1996-05-01

In this work the following studies are concerned: I) preparation of lanthanum, cerium, praseodymium, neodymium and samarium oxides for use as spectro chemically pure standards; II) behavior of the rare earth (La, Ce, Pr, Nd, Sm) carbonates soluble in ammonium carbonate and mixture of ammonium carbonate/ammonium hydroxide, and III) synthesis and characterization of rare earth peroxy carbonates - a new series of compounds. Data for the synthesis and characterization of the rare earths peroxy carbonates described for the first time in this work are presented and discussed. With the aid of thermal analysis (TG-DTG) the thermal stability and the stoichiometric composition for new compounds were established and a mechanism of thermal decomposition was proposed. The peroxy carbonate was prepared by the addition of hydrogen peroxyde to the complexed soluble rare earths carbonates. These studies included also the determinations of active oxygen, the total rare earth oxide by gravimetry and complexometry and the C, H and N contents by microanalysis. The new compounds were also investigated by infrared spectroscopy. (author)

Rare earth impact on glass structure and alteration kinetics

International Nuclear Information System (INIS)

Molieres, E.

2012-01-01

This work is related to the question of the geological deep repository of high-level waste glass. These wastes include fission products and minor actinides, elements which can be simulated by rare earths. As new glass compositions could enable increased rare earth concentrations, it is crucial to know and understand rare earth impact on glass structure on the one hand, and on glass alteration kinetics or their incorporation into an altered layer. This work studied simplified borosilicate glasses in order to limit synergetic effects between rare earths and other elements. Various complementary techniques were used to characterize pristine and altered glasses (solid-high resolution NMR, Raman spectroscopy, fluorescence, SIMS, SAXS). Firstly, the structural role of a rare earth is discussed and is compared to a calcium cation. The local environment of rare earths is also probed. Secondly, rare earth (nature and concentration) impact on several alteration regimes was studied (initial rate, rate drop). Then, after alteration, rare earth elements being retained within the altered layer, the structural impact of rare earth elements (and their local environment) in this alteration layer was also investigated. (author) [fr

Sintered cobalt-rare earth intermetallic product

International Nuclear Information System (INIS)

Benz, M.G.

1975-01-01

This patent describes a sintered product having substantially stable permanent magnet properties in air at room temperature. It comprises compacted particulate cobalt--rare earth alloy consisting essentially of a Co 5 R intermetallic phase and a CoR intermetallic phase which is richer in rare earth metal content than the Co 5 R phase, where R is a rare earth metal. The Co 5 R intermetallic phase is present in an amount of at least 65 percent by weight of the sintered product and the CoR intermetallic phase which is richer in rare earth metal content than the Co 5 R phase is present in a positive amount having a value ranging up to about 35 percent by weight of the product. The sintered product has a density of at least 87 percent and has pores which are substantially noninterconnecting and wherein the component grains have an average size less than 30 microns

Determination of rare earth elements in seawater by inductively coupled plasma-mass spectrometry

International Nuclear Information System (INIS)

Moeller, P.; Dulski, P.; Luck, J.

1992-01-01

Shortly after sampling, rare earth elements (REEs) from 11.5 l of seawater were concentrated in 35 ml solutions by ion exchange chromatography on board the German research vessel ''Sonne'' using Chelex 100 chelating resin for preconcentration. Two millilitres of a 0.2 μg g -1 Lu spike was added to the seawater samples (i) for monitoring the chemical yield which was always found to vary between 85 and 112% (mean: 100±6) and (ii) as an internal standard. Rare earth elements have been determined by ICP-MS, with REE concentrations ranging from 100 (La) to 1 (Eu) pmol kg -1 . La in blanks can be as high as 30 pmol kg -1 , but blank concentrations for other REEs range between 0.5 and 0.01 pmol kg -1 . The trend of the precision of relative response factors varies between 12% (La) and 4% (Yb). The accuracy is estimated to be about 10% with the exception of La and Ce. Methodology improvements are suggested. (author)

Study on Yen Phu rare earth ore concentrate treatment technology and separation of major heavy rare earth elements by solvent extraction method

International Nuclear Information System (INIS)

Le Ba Thuan; Pham Quang Trung; Vu Lap Lai

2003-01-01

1. Yenphu rare earth ore concentrate treatment by alkali under pressure: On the base of studying mineral and chemical compositions of Yenphu rare earth ore concentrate containing 28% TREO and conditions for digestion of ore concentrate by alkali under pressure such as ore concentrate/ NaOH ratio, alkali concentration, pressure and temperature at bench scale (100 gram and 5 kg per batch), the optimal conditions for decomposition of REE ore concentrate have been determined. The yield of the decomposition stage is about 90%. The studies on alkali washing, REE leaching by HCl, pH for leaching process, and iron and radioactive impurities removing by Na 2 S + Na 2 PO 4 have been carried out. The obtained results show that mixture of Na 2 S 5% + Na2PO 4 1% is effective in iron and radioactive impurities removing. The obtained REE oxides get purity of > 99% and meet the need of solvent extraction (SX) individual separation of rare earth elements. The schema for recovery of REEs from Yenphu REE ore concentrate by alkali decomposition under high pressure has been proposed. 2. Fractionation of Yenphu rare earth mixture into subgroups by solvent extraction with PC88A: On the base of simulation program, the parameters for fractional process of rare earths mixture into subgroups by solvent extraction with PC88A have been proposed and determined by experimental verification on mixer-settler set. According to this process, rare earths mixture fractionated into yttrium and light subgroups. In their turn, the light subgroup was separated into light (La, Ce, Pr, Nd) and middle (Sm, Eu, Gd) subgroups. The average yield of the process reached value > 95%. The composition of light subgroup meets the needs for individual separation of Gd, Eu, and Sm. 3. Separation and purification of yttrium: The process for recovery of yttrium consists of two stages: upgrade to get high quality Y concentrate by PC88A and purification by Aliquat 336 in NH 4 SCN-NH 4 Cl medium. The process parameter for

Process for lead removal from rare earth

International Nuclear Information System (INIS)

Bollat, A.; Sabot, J.L.

1987-01-01

An aqueous solution of rare earth chlorides and lead chlorides, with a chloride concentration of at least 2 moles/liter and a pH between 2 and 4, is extracted by an alkylphosphonic acid ester and rare earth(s) is (are) recovered from the organic phase [fr

Red-emitting alkaline-earth rare-earth pentaoxometallates powders ...

Indian Academy of Sciences (India)

Moisture-insensitive metal carboxylates that are mostly liquids at room temperature have been first applied to ... alkaline-earth ion, or possibly even a rare-earth ion and alkali metal ... sion spectra of the powders were recorded on a fluorescent.

Rare earth industries: Upstream business

International Nuclear Information System (INIS)

2011-01-01

Evidently, many factors contribute to the rush to invest in the unprecedented revival of rare earths. One major reason has to do with the rapidly growing world demand. The other reason relates to the attractive price of rare earths which is projected to stay strong in the coming years. This is because supply is predicted to have difficulty keeping pace with demand. Experts believe a major driver of global rare earths demand is the forecasted expansion in the green economy. Climate change is a major driver of the green economy. With climate change, there is concern that the uncontrolled emission of the greenhouse gases, especially carbon dioxide, can lead to catastrophic consequences for the world. This has been documented in countless studies and reports. Another important driver of the green economy is the growing shortfall in many resources. The world is now experiencing declines in key resources to meet a growing global demand. With more than 6 billion people now in the world and growing, the pressure exerted on global resources including energy, water and food is a major concern. Recent demand surge in China and India has dented the supply position of major world resources. The much quoted Stern Report from the UK has warned that, unless immediate steps are taken to reduce greenhouse gas emissions, it may be a costly exercise to undertake the corrections later. Since energy use, especially fossil fuels, is a major contributor to climate change, greener options are being sought. Add to that the fact that the fossil energy resources of the world are declining, the need to seek alternatives becomes even more urgent. One option is to change to renewable energy sources. These include such potentials as solar, wind and biomass. Rare earths have somehow become a critical feature of the technologies in such renewable. Another option is to improve the efficient use of energy in transport, buildings and all the other energy intensive industries. Again the technologies in

Rare earth - no case for government intervention

OpenAIRE

Georg Zachmann

2010-01-01

China has officially restricted exports of rare earth for several years and announced this year it will further tighten exports. Rare earth is a group of 17 different metals, usually found clustered together. These metals have hundreds of different industry applications. For example, they are used in certain high capacity magnets, batteries and lasers. As the rare earth elements are used in sectors that are assumed to have an over-proportionate growth potential (eg. green-technology), policy ...

Magnetic properties of RT₂Zn₂₀; R = rare earth, T = Fe, Co, Ru, Os and Ir

Energy Technology Data Exchange (ETDEWEB)

Jia, Shuang [Ames Lab. and Iowa State Univ., Ames, IA (United States)

2008-01-01

It is well known that rare earth intermetallic compounds have versatile, magnetic properties associated with the 4f electrons: a local moment associated with the Hund's rule ground state is formed in general, but a strongly correlated, hybridized state may also appear for specific 4f electronic configuration (eg. for rare earth elements such as Ce or Yb). On the other hand, the conduction electrons in rare earth intermetallic compounds, certainly ones associated with non hybridizing rare earths, usually manifest non-magnetic behavior and can be treated as a normal, non-interacted Fermi liquid, except for some 3d-transition metal rich binary or ternary systems which often manifest strong, itinerant, d electron dominant magnetic behavior. Of particular interest are examples in which the band filling of the conduction electrons puts the system in the vicinity of a Stoner transition: such systems, characterized as nearly or weakly ferromagnet, manifest strongly correlated electronic properties [Moriya, 1985]. For rare earth intermetallic compounds, such systems provide an additional versatility and allow for the study of the behaviors of local moments and hybridized moments which are associated with 4f electron in a correlated conduction electron background.

Precipitation of the rare earth double sodium and rare earths from the sulfuric liquor and the conversion into rare earth hydroxides through meta ethic reaction

International Nuclear Information System (INIS)

Abreu, Renata D.; Oliveira, Ester F.; Brito, Walter de; Morais, Carlos A.

2007-01-01

This work presents the purification study of the rare earths through precipitation of rare earth and sodium (Na TR (SO 4 ) 2 . x H 2 O)) double sulfate and his conversion to rare earths hydroxide TR(OH) 3 by meta ethic reaction through the addition of sodium hydroxide solution to the solid double sulfate. The study used the sulfuric liquor as rare earth sample, generated in the chemical processing of the monazite with sulfuric acid by the Industrias Nucleares do Brasil - INB, Brazil, after the thorium and uranium extraction. The work investigated the influence of the main variables involved in the precipitation of Na TR(SO 4 ) 2 .xH 2 O and in the conversion for the TR(OH) 3 , as follows: type and excess of the precipitation agent, temperature and time reaction. The obtained solid composites were characterized by X-ray diffraction, infrared and chemical analysis. The double sulfate diffractogram indicated the Na TR(SO 4 ) 2 mono-hydrated. The characterization of the metatese products has shown that, for obtaining the complete conversion of NaTR(SO 4 ) 2 .H 2 O into TR(OH) 3 , the reaction must be hot processed (∼70 deg C) and with small excess of Na OH (≤ 5 percent). (author)

Luminescence of rare-earth ions in Mg[sub 2]SiO[sub 4

Energy Technology Data Exchange (ETDEWEB)

Van der Voort, D; Maat-Gersdorf, I de; Blasse, G [Rijksuniversiteit Utrecht (Netherlands)

1992-01-01

The luminescence of the rare-earth ions Eu[sup 3+], Tb[sup 3+] and Ce[sup 3+] in Mg[sub 2]SiO[sub 4] is reported. The Tb[sup 3+] ion shows a change in emission colour from blue to green depending on the charge compensator. This is ascribed to a difference in coupling of the Tb[sup 3+] ion to the vibrational lattice modes. The Eu[sup 3+] ion has an average quantum efficiency under charge-transfer excitation of 60% at 4.2 and 20% at 300 K. The Ce[sup 3+] emission is situated in the blue and shows a Stokes shift of 3 500 cm[sup -1]. The relaxation of these ions in the excited state is discussed in terms of their positive effective charge and the stiffness of their surroundings.

Rare (Earth Elements [score

Directory of Open Access Journals (Sweden)

Camilo Méndez

2014-12-01

Full Text Available Rare (Earth Elements is a cycle of works for solo piano. The cycle was inspired by James Dillon’s Book of Elements (Vol. I-V. The complete cycle will consist of 14 pieces; one for each selected rare (earth element. The chosen elements are Neodymium, Erbium, Tellurium, Hafnium, Tantalum, Technetium, Indium, Dysprosium, Lanthanium, Cerium, Europium, Terbium, Yttrium and Darmstadtium. These elements were selected due to their special atomic properties that in many cases make them extremely valuable for the development of new technologies, and also because of their scarcity. To date, only 4 works have been completed Yttrium, Technetium, Indium and Tellurium.

An Overview of Rare Earth Science and Technology

Science.gov (United States)

Gschneidner, Karl, Jr.

2012-02-01

Currently rare earth science and technology is robust: this includes all the major branches of science -- biochemistry, chemistry, materials and physics. There are, however, currently some anomalies and distortions especially in the technology and applications sector of the rare earth field, which is caused by the dominance of China on the sales of rare earths and rare earth containing products. For the past 5 to 10 years ˜95% of rare earths utilized in commerce came from China. Although Chinese actions have lead to sudden and large price spikes and export embargoes, the rare earths are still available but at a higher cost. The start up of production in 2011 at mines in the USA and Australia will alleviate this situation in about two years. Basic and applied research on the condensed matter physics/materials science has hardly been impacted by these events, but new research opportunities are opening up especially with regard to the USA's military and energy security. Magnets seems to be the hottest topic, but research on battery materials, phosphors and catalysts are also (or should be) strongly considered.

Determination of rare earths in their extraction processing

International Nuclear Information System (INIS)

You Jiannan; Zhang Yuqin

1989-01-01

A method for determination of rare earths in ores, ion-exchange resins and solution samples has been developed. The ore is molten with sodium peroxide and the molten sample is leached with triethenol amine and sodium citrate. In weak acid medium, the rare earths can be extracted by PMBP-phenol solution, and stripped with formic acid. In the acetic acidsodium acetate buffer medium of pH3, the spectrophotometric determination of rare earths with arsenazo M has been made. The rare earths in ion-exchange resins can be directly determined by spectrophotometry after being leached with hydrochloric acid and at heated condition. The rare earths with arsenazo M or a red complex. The maximum absorption of the complex is at 640 nm, and the molar absorption is 8.0 x 10 4 L centre dot mol -1 centre dot cm -1 . While the range of determination is 0.005%-0.5% and 0.001-1.0 g/L, the relative standard deviation is less than 5%, and recovery of rare earths is 98.5-105%. The method is rather simple and rapid

High purity samarium oxide from mixed rare earth carbonates

International Nuclear Information System (INIS)

Queiroz, Carlos A. da S.; Seneda, Jose A.; Vasconcellos, Mari E. de; Pedreira Filho, Walter dos R.

2013-01-01

A simple and economical chemical process for the production of highly pure samarium oxides is discussed. The raw material, which was used in the form of rare earth carbonates was produced industrially from the chemical treatment of Brazilian monazite. Ion exchange chromatography was performed using a strong cationic resin that is typically employed in water treatment processes to fractionate rare earth elements (REE) without the use of retention ions. Under these conditions, 99.9% pure Sm 2 O 3 was eluted using the ammonium salt of ethylenediaminetetraacetic acid (EDTA) at a controlled pH. The EDTA-samarium complex was separated from EDTA and then precipitated as oxalate and fired to samarium oxide. Molecular absorption spectrophotometry was used to monitor the samarium content during the proposed process, and sector field inductively coupled plasma mass spectrometry was used to certify the purity of the samarium oxide. Typical samarium oxide obtained from the proposed procedure contained the following contaminants in micrograms per gram: Sc (20.90); Y (11.80); La (8.4); Ce (4.3); Pr (2.5); Nd (5.1); Eu (94); Gd (114); Tb (3.6); Dy (2.5), Ho (2.3); Er (3.0); Tm (2.3); Yb (38,2); Lu (25.6). The high-purity samarium oxides produced in the present study can be used as an alternative to imported products in research and development applications. (author)

State of rare earth impurities in gallium and indium antimonides

International Nuclear Information System (INIS)

Evgen'ev, S.B.; Kuz'micheva, G.M.

1990-01-01

State of rare earth impurities in indium and gallium antimonides was studied. Results of measuring density and lattice parameter of samples in GaSb-rare earth and InSb-rare earth systems are presented. It is shown that during rare earth dissolution in indium and gallium antimonides rare earth atoms occupy interstitial positions or, at least, are displaced from lattice points

Metal nitride cluster as a template to tune the electronic and magnetic properties of rare-earth metal containing endohedral fullerenes

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yang

2013-10-16

Rare-earth metal containing endohedral fullerenes have attracted much attention due to the feasibility of encaging metal atom, atoms or cluster inside of carbon cages. By switching the metal atom or cluster entrapped inside of the carbon cage the physical and chemical properties of the fullerene compounds can be tuned. The understanding of magnetic and electrochemical properties of endohedral fullerenes plays an essential role in fundamental scientific researches and potential applications in materials science. In this thesis, synthesizing novel rare-earth metal containing endohedral fullerene structures, studying the properties of these isolated endohedral fullerenes and the strategies of tuning the electronic and magnetic properties of endohedral fullerenes were introduced. The DC-arc discharging synthesis of different lanthanide metal-based (Ho, Ce and Pr) mixed metal nitride clusterfullerenes was achieved. Those rare-earth metal containing endohedral fullerenes were isolated by multi-step HPLC. The isolated samples were characterized by spectroscopic techniques included UV-vis-NIR, FTIR, Raman, LDI-TOF mass spectrometry, NMR and electrochemistry. The Ho-based mixed metal nitride clusterfullerenes Ho{sub x}M{sub 3-x}N rate at C{sub 80} (M= Sc, Lu, Y; x=1, 2) were synthesized by ''reactive gas atmosphere'' method or ''selective organic solid'' route. The isolated samples were characterized by LDI-TOF mass spectrometry, UV-vis-NIR, FTIR, Raman and NMR spectroscopy. The {sup 13}C NMR spectroscopic studies demonstrated exceptional NMR behaviors that resulted from switching the second metal inside of the mixed metal nitride cluster Ho{sub x}M{sub 3-x}N from Sc to Lu and further to Y. The LnSc{sub 2}N rate at C{sub 80} (Ln= Ce, Pr, Nd, Tb, Dy, Ho, Lu) MMNCFs were characterized by {sup 13}C and {sup 45}Sc NMR study respectively. According to Bleaney's theory and Reilley method, the separation of δ{sup PC} and δ{sup con

The formation of crystals in glasses containing rare earth oxides

Energy Technology Data Exchange (ETDEWEB)

Fadzil, Syazwani Mohd [Pohang University of Science and Technology (POSTECH), Pohang (Korea, Republic of); Hrma, Pavel [Pohang University of Science and Technology (POSTECH), Pohang, South Korea and Pacific Northwest National Laboratory, Richland, Washington (United States); Crum, Jarrod [Pacific Northwest National Laboratory, Richland, Washington (United States); Siong, Khoo Kok; Ngatiman, Mohammad Fadzlee; Said, Riduan Mt [National University of Malaysia, Bandar Baru Bangi, Selangor (Malaysia)

2014-02-12

Korean spent nuclear fuel will reach the capacity of the available temporary storage by 2016. Pyroprocessing and direct disposal seems to be an alternative way to manage and reuse spent nuclear fuel while avoiding the wet reprocessing technology. Pyroprocessing produces several wastes streams, including metals, salts, and rare earths, which must be converted into stabilized form. A suitable form for rare earth immobilization is borosilicate glass. The borosilicate glass form exhibits excellent durability, allows a high waste loading, and is easy to process. In this work, we combined the rare earths waste of composition (in wt%) 39.2Nd{sub 2}O{sub 3}–22.7CeO{sub 2}–11.7La{sub 2}O{sub 3}–10.9PrO{sub 2}–1.3Eu{sub 2}O{sub 3}–1.3Gd{sub 2}O{sub 3}–8.1Sm{sub 2}O{sub 3}–4.8Y{sub 2}O{sub 3} with a baseline glass of composition 60.2SiO{sub 2}–16.0B{sub 2}O{sub 3}–12.6Na{sub 2}O–3.8Al{sub 2}O{sub 3}–5.7CaO–1.7ZrO{sub 2}. Crystallization in waste glasses occurs as the waste loading increases. It may produce complicate glass processing and affect the product quality. To study crystal formation, we initially made glasses containing 5%, 10% and 15% of La{sub 2}O{sub 3} and then glasses with 5%, 10% and 15% of the complete rare earth mix. Samples were heat-treated for 24 hours at temperatures 800°C to 1150°C in 50°C increments. Quenched samples were analyzed using an optical microscope, scanning electron microscope with energy dispersive spectroscopy, and x-ray diffraction. Stillwellite (LaBSiO{sub 5}) and oxyapatite (Ca{sub 2}La{sub 8}Si{sub 6}O{sub 26}) were found in glasses containing La{sub 2}O{sub 3}, while oxyapatite (Ca{sub 2}La{sub 8}Si{sub 6}O{sub 26} and NaNd{sub 9}Si{sub 6}O{sub 26}) precipitated in glasses with additions of mixed rare earths. The liquidus temperature (T{sub L}) of the glasses containing 5%, 10% and 15% La{sub 2}O{sub 3} were 800°C, 959°C and 986°C, respectively; while T{sub L} was 825°C, 1059°C and 1267°C for glasses

Monazite upgradation and production of high pure rare earths

International Nuclear Information System (INIS)

Asnani, C.K.; Mohanty, D.; Kumar, S.S.

2014-01-01

Rare earth extraction from monazite and further processing of mixed rare earth chlorides for producing individual high pure rare earths involves a complex flowsheet based on solvent extraction process. Apart from involving multiple extractions, scrubbing and stripping operations, the flowsheet requires optimization of critical parameters such as solvent molarity, solvent saponification level and recycling of product solutions as reflux to ensure preferential upload of required rare earths to generate high purity product. This paper tracks monazite flow from the raw sand feed through to the monazite product and its processing to generate rare earths of internationally acceptable quality

Rare earth oxyhydrides and preparation process

International Nuclear Information System (INIS)

Diaz, H.

1986-01-01

Rare earth oxyhydrides of formula RE 1-q Th q Ni 5-p M p O x H y are claimed. RE is a rare earth, Th can be replaced by Yt, M is Cu, Mn, Al, Fe, Cr or Co, o O C and the hydrides are oxidized. They are catalysts for various chemical reactions [fr

Rare Earth Elements Distribution in Beryl

International Nuclear Information System (INIS)

El Gawish, H.K.; Nada, N.; Ghaly, W.A.; Helal, A.I.

2012-01-01

Laser ablation method is applied to a double focusing inductively coupled plasma mass spectrometer to determine the rare earth element distribution in some selected beryl samples. White, green and blue beryl samples are selected from the Egyptian eastern desert. Distributions of chondrite- normalized plot for the rare earth element in the selected beryl samples are investigated

Rare Earth-Activated Silica-Based Nanocomposites

Directory of Open Access Journals (Sweden)

C. Armellini

2007-01-01

Full Text Available Two different kinds of rare earth-activated glass-based nanocomposite photonic materials, which allow to tailor the spectroscopic properties of rare-earth ions: (i Er3+-activated SiO2-HfO2 waveguide glass ceramic, and (ii core-shell-like structures of Er3+-activated silica spheres obtained by a seed growth method, are presented.

Rare earth intermetallic compounds produced by a reduction-diffusion process

International Nuclear Information System (INIS)

Cech, R.E.

1975-01-01

A reduction-diffusion process is given for producing novel rare earth intermetallic compounds, such as cobalt--rare earth intermetallic compounds, especially compounds useful in preparing permanent magnets. A particulate mixture of rare earth metal halide, cobalt and calcium hydride is heated to effect reduction of the rare earth metal halide and to diffuse the resulting rare earth metal into the cobalt to form the intermetallic compound

Bioleaching of rare earth elements from monazite sand.

Science.gov (United States)

Brisson, Vanessa L; Zhuang, Wei-Qin; Alvarez-Cohen, Lisa

2016-02-01

Three fungal strains were found to be capable of bioleaching rare earth elements from monazite, a rare earth phosphate mineral, utilizing the monazite as a phosphate source and releasing rare earth cations into solution. These organisms include one known phosphate solubilizing fungus, Aspergillus niger ATCC 1015, as well as two newly isolated fungi: an Aspergillus terreus strain ML3-1 and a Paecilomyces spp. strain WE3-F. Although monazite also contains the radioactive element Thorium, bioleaching by these fungi preferentially solubilized rare earth elements over Thorium, leaving the Thorium in the solid residual. Adjustments in growth media composition improved bioleaching performance measured as rare earth release. Cell-free spent medium generated during growth of A. terreus strain ML3-1 and Paecilomyces spp. strain WE3-F in the presence of monazite leached rare earths to concentrations 1.7-3.8 times those of HCl solutions of comparable pH, indicating that compounds exogenously released by these organisms contribute substantially to leaching. Organic acids released by the organisms included acetic, citric, gluconic, itaconic, oxalic, and succinic acids. Abiotic leaching with laboratory prepared solutions of these acids was not as effective as bioleaching or leaching with cell-free spent medium at releasing rare earths from monazite, indicating that compounds other than the identified organic acids contribute to leaching performance. © 2015 Wiley Periodicals, Inc.

Review on dielectric properties of rare earth doped barium titanate

International Nuclear Information System (INIS)

Ismail, Fatin Adila; Osman, Rozana Aina Maulat; Idris, Mohd Sobri

2016-01-01

Rare earth doped Barium Titanate (BaTiO_3) were studied due to high permittivity, excellent electrical properties and have wide usage in various applications. This paper reviewed on the electrical properties of RE doped BaTiO_3 (RE: Lanthanum (La), Erbium (Er), Samarium (Sm), Neodymium (Nd), Cerium (Ce)), processing method, phase transition occurred and solid solution range for complete study. Most of the RE doped BaTiO_3 downshifted the Curie temperature (T_C). Transition temperature also known as Curie temperature, T_C where the ceramics had a transition from ferroelectric to a paraelectric phase. In this review, the dielectric constant of La-doped BaTiO_3, Er-doped BaTiO_3, Sm-doped BaTiO_3, Nd-doped BaTiO_3 and Ce-doped BaTiO_3 had been proved to increase and the transition temperature or also known as T_C also lowered down to room temperature as for all the RE doped BaTiO_3 except for Er-doped BaTiO_3.

Rare earth elements materials production from apatite ores

International Nuclear Information System (INIS)

Anufrieva, A V; Buynovskiy, A S; Makaseev, Y N; Mazov, I N; Nefedov, R A; Sachkov, V I; Valkov, A V; Andrienko, O S; Stepanova, O B

2016-01-01

The paper deals with the study of processing apatite ores with nitric acid and extraction of the rare earth elements. The rare earth elements can be successfully separated and recovered by extraction from the nitrate- phosphate solution, being an tributyl phosphate as extraction agent. The developed scheme of the processing apatite concentrate provides obtaining rare earth concentrates with high qualitative characteristics. (paper)

On the corrosion of binary magnesium-rare earth alloys

Energy Technology Data Exchange (ETDEWEB)

Birbilis, N. [ARC Centre of Excellence for Design in Light Metals, Monash University (Australia); CAST Co-operative Research Centre (Australia); Department of Materials Engineering, Monash University, Wellington Road, Clayton, Vic. 3800 (Australia)], E-mail: nick.birbilis@eng.monash.edu.au; Easton, M.A. [CAST Co-operative Research Centre (Australia); Department of Materials Engineering, Monash University, Wellington Road, Clayton, Vic. 3800 (Australia); Sudholz, A.D. [ARC Centre of Excellence for Design in Light Metals, Monash University (Australia); Department of Materials Engineering, Monash University, Wellington Road, Clayton, Vic. 3800 (Australia); Zhu, S.M. [CAST Co-operative Research Centre (Australia); Department of Materials Engineering, Monash University, Wellington Road, Clayton, Vic. 3800 (Australia); Gibson, M.A. [CAST Co-operative Research Centre (Australia); CSIRO Division of Materials Science and Engineering (Australia)

2009-03-15

The corrosion properties of high-pressure die cast (HPDC) magnesium-rare earth (RE) based alloys have been studied. Binary additions of La, Ce and Nd to commercially pure Mg were made up to a nominal 6 wt.%. It was found that the intermetallic phases formed in the eutectic were Mg{sub 12}La, Mg{sub 12}Ce and Mg{sub 3}Nd, respectively. Results indicated that increasing RE alloying additions systematically increased corrosion rates. This was also described in the context of the electrochemical response of Mg-RE intermetallics - which were independently assessed by the electrochemical microcapillary technique. This study is a discrete effort towards revealing the electrochemical effect of carefully controlled binary alloying additions to magnesium in order to elucidate the microstructure-corrosion relationship more generally for HPDC Mg alloys. Such fundamental information is seen to not only be useful in understanding the corrosion of alloys which presently contain RE additions, but may be exploited in the design of magnesium alloys with more predictable corrosion behaviour. There is a special need to understand this relationship - particularly for magnesium that commonly displays poor corrosion resistance.

Continental shelves as potential resource of rare earth elements.

Science.gov (United States)

Pourret, Olivier; Tuduri, Johann

2017-07-19

The results of this study allow the reassessment of the rare earth elements (REE) external cycle. Indeed, the river input to the oceans has relatively flat REE patterns without cerium (Ce) anomalies, whereas oceanic REE patterns exhibit strong negative Ce anomalies and heavy REE enrichment. Indeed, the processes at the origin of seawater REE patterns are commonly thought to occur within the ocean masses themselves. However, the results from the present study illustrate that seawater-like REE patterns already occur in the truly dissolved pool of river input. This leads us to favor a partial or complete removal of the colloidal REE pool during estuarine mixing by coagulation, as previously shown for dissolved humic acids and iron. In this latter case, REE fractionation occurs because colloidal and truly dissolved pools have different REE patterns. Thus, the REE patterns of seawater could be the combination of both intra-oceanic and riverine processes. In this study, we show that the Atlantic continental shelves could be considered potential REE traps, suggesting further that shelf sediments could potentially become a resource for REE, similar to metalliferous deep sea sediments.

Nanocrystalline Mn-Mo-Ce Oxide Anode Doped Rare Earth Ce and Its Selective Electro-catalytic Performance

Directory of Open Access Journals (Sweden)

SHI Yan-hua

2017-09-01

Full Text Available The anode oxide of nanocrystalline Mn-Mo-Ce was prepared by anode electro-deposition technology, and its nanostructure and selective electro-catalytic performance were investigated using the SEM, EDS, XRD, HRTEM, electrochemical technology and oxygen evolution efficiency testing. Furthermore, the selective electro-catalytic mechanism of oxygen evolution and chlorine depression was discussed. The results show that the mesh-like nanostructure Mn-Mo-Ce oxide anode with little cerium doped is obtained, and the oxygen evolution efficiency for the anode in the seawater is 99.51%, which means a high efficiency for the selective electro-catalytic for the oxygen evolution. Due to the structural characteristics of γ-MnO2, the OH- ion is preferentially absorbed, while Cl- absorption is depressed. OH- accomplishes the oxygen evolution process during the valence transition electrocatalysis of Mn4+/Mn3+, completing the selective electro-catalysis process. Ce doping greatly increases the reaction activity, and promotes the absorption and discharge; the rising interplanar spacing between active (100 crystalline plane promotes OH- motion and the escape of newborn O2, so that the selective electro-catalytic property with high efficient oxygen evolution and chlorine depression is achieved from the nano morphology effect.

Rare earth industries; Moving Malaysia's Green Economy Forward

International Nuclear Information System (INIS)

2011-08-01

There is a famous saying, Where there is risk, there is opportunity. Rare earths present both health and environmental risks as well as potential economic opportunities. However, the risks are manageable thanks to improved technologies and a better understanding of the implications on health and the environment. This explains why there is a rush by many countries to reopen old mines and increase investment in the production of rare earths concentrate and their high value downstream products. Why is there such a scramble to risk money on rare earths? What have ignited global demand? Where are the opportunities? How are the risks associated with rare earths managed? Can Malaysia benefit from this new growth industry? What should be our strategies? This report, produced by the joint Working Group of the Academy of Sciences Malaysia (ASM) and the Majlis Professor Negara (MPN), discusses the science of rare earths and their business prospects; and proposes some strategic directions for Malaysia. The analysis is based on information culled from various secondary sources as well as the groups engagement with experts from the Rare Earths Society of China. (author)

Characterization of three Brazilian bauxites and the corresponding bayer liquors in regard to rare earth and other minor elements

International Nuclear Information System (INIS)

Ikeda Oba, C.A.; Avritscher, W.; Pini, R.A.; Abrao, A.; Chaves, A.P.

1998-01-01

Full text: In this paper the results of chemical analysis of representative Brazilian bauxites are presented and discussed. Analyses were made on original mother rocks, ores, tailings from washing plants, Bayer liquors produced from this ores and also from the red muds. Samples of the ores were submitted to size, magnetic and density separation and these fractions were also analysed. Minor elements of interest assayed were rare earth, gallium and vanadium. Atomic absorption spectroscopy, x-ray fluorescence and emission spectroscopy were applied for the minor elements and also conventional wet chemical analyses mainly for major elements. A special technique for a rapid identification and semi-quantitative analysis of gallium and a permanent file for the results are presented as well. Brazilian bauxites are all of lateritic origin, constituted essentially by gibbsite and formed by intense tropical weathering of different rocks. This paper presents the chemical characterization of three Brazilian bauxites, namely Porto Trombetas, Cataguazes and Pocos de Caldas and the behaviour of their minor elements during the industrial processing in the mines and alumina mills. The grades of rare earths elements, gallium and vanadium show significant variations. This is most probably due to mother rocks characteristics than to bauxitization processes. The review deposits have the following mother rocks: Porto Trombetas Sedimentary - Cataguazes Metamorphic - Pocos de Caldas Alkaline (sienite). The samples from Pocos de Caldas show high grade for La+Ce with an average over 800ppm, Cataguazes has an average of 76 ppm La+Ce and Porto Trombetas 6,5ppm. Gallium grades are higher for Pocos de Caldas (average 135 ppm), followed by Porto Trombetas (62 ppm) and Cataguazes (37ppm). Vanadium grades are higher for Porto Trombetas (243 ppm) then Pocos de Caldas (165 ppm). Pocos de Caldas shows 50% enrichment in Ce in the washed ore and in Porto Trombetas most of the Y goes to the fines (product

Enzymatic determination of rare earth elements using pyrophosphatases

International Nuclear Information System (INIS)

Shekhovtsova, T.N.; Pirogova, S.V.; Fedorova, O.M.; Dolmanova, I.F.; Bajkov, A.A.

1993-01-01

A highly sensitive(determination limit 8x10 -6 -4x10 -4 μ g/m) and selective enzymatic method for determination of rare earth elements has been developed. The method is based on inhibition action of rare earths on the catalytic activity of pyrophosphates isolated from bakery geast and E.Coli. The mechanism of the rare earth element action, corresponding to competitive inhibition, has been established

Optical properties of pure and Ce3+ doped gadolinium gallium garnet crystals and epitaxial layers

International Nuclear Information System (INIS)

Syvorotka, I.I.; Sugak, D.; Wierzbicka, A.; Wittlin, A.; Przybylińska, H.; Barzowska, J.; Barcz, A.; Berkowski, M.; Domagała, J.; Mahlik, S.; Grinberg, M.; Ma, Chong-Geng

2015-01-01

Results of X-ray diffraction and low temperature optical absorption measurements of cerium doped gadolinium gallium garnet single crystals and epitaxial layers are reported. In the region of intra-configurational 4f–4f transitions the spectra of the bulk crystals exhibit the signatures of several different Ce 3+ related centers. Apart from the dominant center, associated with Ce substituting gadolinium, at least three other centers are found, some of them attributed to the so-called antisite locations of rare-earth ions in the garnet host, i.e., in the Ga positions. X-ray diffraction data prove lattice expansion of bulk GGG crystals due to the presence of rare-earth antisites. The concentration of the additional Ce-related centers in epitaxial layers is much lower than in the bulk crystals. However, the Ce-doped layers incorporate a large amount of Pb from flux, which is the most probable source of nonradiative quenching of Ce luminescence, not observed in crystals grown by the Czochralski method. - Highlights: • Ce 3+ multicenters found in Gadolinium Gallium Garnet crystals and epitaxial layers. • High quality epitaxial layers of pure and Ce-doped GGG were grown. • Luminescence quenching of Ce 3+ by Pb ions from flux detected in GGG epitaxial layers. • X-ray diffraction allows measuring the amount of the rare-earth antisites in GGG

Preliminary study on the existence characteristics of rare earth elements in the interstratified oxidized zone

International Nuclear Information System (INIS)

Wang Jinping

2006-10-01

There were few of studies on rare earth elements (REE) in sandstone hosted uranium deposits, except the study of sediments source tracing and REE distribution modalities. Based on the study of existence characteristics of REE in subzones of interstratified oxidized zone in Shihongtan uranium deposit, Tuha basin, the possible migration features of REE was traced, and the significance of ΣREE, LREE/HREE ratios and δEu, δCe value during the interstratified oxidation were illustrated. (authors)

A Study on Electrochemical Reduction of Rare Earth Oxides in Molten LiCl-Li2O Salt

International Nuclear Information System (INIS)

Lee, Min Woo; Jeong, Sang Mun; Lee, See Hoon; Sohn, Jung Min

2016-01-01

In this study, the electrochemical reduction of RE 2 O 3 (RE = Nd or Ce) has been conducted via co-reduction NiO to increase the reduction degree of the rare earth oxides in molten molten LiCl containing 1wt% Li 2 O. The electrochemical reduction behavior of the mixed RE 2 O 3 -NiO oxide has been investigated and the reduction path of RE 2 O 3 has been proposed. An electorchemical spent fuel processing technology, pyroprocessing, has been developed for recycling of spent fuel to be applied to a sodium-cooled fast reactor. The spent fuel is reduced in the oxide reduction process. It is well known that the rare earth oxides are hardly reduced due to their electrochemical and thermodynamic stability. The rare earth oxides unreduced in the reduction process can cause problems via reaction with UCl 3 in the electrorefiner. To tackle those problems, the electrochemical reduction of rare earth oxide has been conducted via co-reduction of NiO in LiCl molten salt containing 1 wt% Li 2 O. The reduction of the oxide mixture starts from the reduction of NiO to Ni, followed by that of RE 2 O 3 on the produced Ni to form intermetallic RENi 5 . The mixed oxide pellets were successfully reduced to the RENi5 alloy by constant electrolysis at 3.0 V at 650 .deg. C. The crucial aspect to these results is that the thermodynamically stable rare-earth oxide, Nd 2 O 3 was successfully converted to the metal in the presence of NiO.

Rare Earth Elements (La, Ce, Pr, Nd, and Sm from a Carbonatite Deposit: Mineralogical Characterization and Geochemical Behavior

Directory of Open Access Journals (Sweden)

Mohamed Edahbi

2018-02-01

Full Text Available Geochemical characterization including mineralogical measurements and kinetic testing was completed on samples from the Montviel carbonatite deposit, located in Quebec (Canada. Three main lithological units representing both waste and ore grades were sampled from drill core. A rare earth element (REE concentrate was produced through a combination of gravity and magnetic separation. All samples were characterized using different mineralogical techniques (i.e., quantitative evaluation of minerals by scanning electron microscopy (QEMSCAN, X-ray diffraction (XRD, and scanning electron microscopy with X-ray microanalysis (SEM-EDS in order to quantify modal mineralogy, liberation, REE deportment and composition of REE-bearing phases. The REE concentrate was then submitted for kinetic testing (weathering cell in order to investigate the REE leaching potential. The mineralogical results indicate that: (i the main REE-bearing minerals in all samples are burbankite, kukharenkoite-Ce, monazite, and apatite; (ii the samples are dominated by REE-free carbonates (i.e., calcite, ankerite, and siderite; and (iii LREE is more abundant than HREE. Grades of REE minerals, sulfides and oxides are richer in the concentrate than in the host lithologies. The geochemical test results show that low concentrations of light REE are leached under kinetic testing conditions (8.8–139.6 µg/L total light REE. These results are explained by a low reactivity of the REE-bearing carbonates in the kinetic testing conditions, low amounts of REE in solids, and by precipitation of secondary REE minerals.

Geochemical and rare earth elements distribution pattern in gaiman F M.phosphatic levels, Chubu t, Argentina

International Nuclear Information System (INIS)

Castro, L.; Fazio, A.; Tourn, S.; Scasso, R.

2004-01-01

Phosphatic concretions in the Early Miocene marine sediments of the Gaiman Formation (Miocene) were analyzed for rare earth elements (REE), in order to discuss their pattern in the context of paleoenvironmental interpretations. P2O5 in concretions is between 15,61 to 21,82%. Two types of concretions are found: Type 1 represented by in situ ones developed within transgressive-early highstand system tracts which shows little evidence for significant transportation, and Type 2 related to reworking, winnowing and mechanical concentration of resistant particles. Type 1 exhibits higher REE/P ratios and a significant enrichment in HREE than Type 2. The REE pattern in both shows a slight depletion in LREE with a weak Ce anomaly (-0.08 to 0.04), and an enrichment in high rare earth elements, in comparison to the a verage shale. Their mean content in REE (915 ppm) and Y (500 ppm) doubles the worldwide phosphorite average (462 ppm and 275 ppm). No significant correlation is found between REEs and P2O5. On the other hand, HREE enrichment (Lu/Ce) increases with the REEs bulk content. The pattern is consistent with shallow water inner shelf marine environment which is also suggested by sedimentological and paleontological evidence [es

12 Ministries Control Rare Earth Exports

Institute of Scientific and Technical Information of China (English)

2010-01-01

<正>"It is very natural to reserve rare earth as a strategic resource.Many countries do this,including China."On April 8,Sun Lihui,Vice Director of Metal Section of Chemicals Import & Export Commerce Chamber of China Minmetals Corporation told a reporter that as early as 2006,China has launched a strategic plan for rare earth,"but it was interrupted by the subsequent financial crisis."

Emerging industrial processes for low grade rare earth mineral concentrates

International Nuclear Information System (INIS)

Soldenhoff, Karin; Ho, Elizabeth

2015-01-01

Historically rare earth recovery has mainly been derived from the processing of monazite, bastnasite and xenotime containing ores amenable to beneficiation, yielding high grade mineral concentrates. A notable exception is the recovery of heavy rare earths from ionic clays in Southern China. Recently, projects are being proposed to treat a range of mineral concentrates which tend to be lower grade with wide ranging modal mineralogy for rare earths and associated gangue minerals. This has a significant impact on processing routes. This paper discusses processes proposed for emerging rare earth producers and how different projects have responded to particular challenges including: Control of phosphorous due to the presence of xenotime or monazite type minerals; Control of phosphorous due to the presence of rare earth containing apatite; Rare earth recovery from polymetallic ores; Control of radionuclides in rare earth processing, etc.

Thermogravimetric study of rare earth concentrates

International Nuclear Information System (INIS)

Delyagejd, V.V.; Anisimova, V.N.; Eremenko, Z.V.; Kutsev, V.S.

1974-01-01

Methods of thermogravimetric, chemical and phase analysis were used in measuring the concentration of rare-earth elements of different origins. At temperatures 400-800 deg C a gradual decomposition of fluorocarbonates takes place leading to the formation of derivatives of corresponding oxides and oxyfluorides. For concentrates containing siderite the process takes place at 550-600 deg C followed by oxidation of bivalent iron into trivalent state. Reaction of rare-earth elements with sodium carbonate and the increase in the concentration of the latter results in a narrowing down of the interval of temperatures at which decomposition takes place. Under these conditions an intense reaction and a fusion take place leading to the formation of eutectic at 500-600 deg C and further synthesis of sodium fluoride and oxyfluoride derivatives of calcium and rare-earth elements

Neutron-activation determination of the rare earths in natural calcites using a semiconductor detector

International Nuclear Information System (INIS)

Vaganov, N.A.; Bulnaev, A.I.; Mejer, V.A.; Ponomarev, V.S.

1976-01-01

The application of germanium semiconducting detector is described. The detector has an energy resolution about 1 KeV and makes it possible to determine the content of Ce, Nd, Eu, Gd, Tb, and Yb in natural calcites with high sensitivity. The region of soft γ-radiation of activated calcites is more favourable for measurements to be performed than the region of hard γ-rays. Semiconducting detectors of radiation type are relatively cheap; they can be stored at room temperature. The limit of determining rare earth elements in calcites is (g): Eu-1.5.10 -9 ; Tb-4.0.10 -9 ; Yb-7.0.10 -9 ; Ce-1.0.10 -7 ; Nd-5.0.10 -7 ; Gd-1.0.10 -6 . A relative error of concentration determination is 10-20%

Investigation on fuel-cladding chemical interaction in metal fuel for FBR. Reaction of rare earth elements with Fe-Cr alloy

International Nuclear Information System (INIS)

Inagaki, Kenta; Ogata, Takanari

2010-01-01

Rare-earth fission product (FP) elements generated in the metal fuel interact with cladding alloy and result in the wastage of the cladding (Fuel-Cladding Chemical Interaction (FCCI)). To evaluate FCCI quantitatively, several influential factors must be considered. They are temperature, temperature gradient, time, composition of the cladding and the behavior of rare-earth FP. In this research, the temperature and time dependencies are investigated with tests in the simplified system. Fe-12wt%Cr was used as stimulant material of cladding and rare-earth alloy 13La -24Ce -12Pr -39Nd -12Sm (RE) as a rare-earth FP. A diffusion couple Fe-Cr/RE was made and annealed at 923K, 853K, 773K or 693K. The structures of reaction layers were analyzed with Electron Probe Micro Analyzer (EPMA) and the details of the structures were clarified. The width of the reaction layer in the Fe-Cr alloy grew in proportion to the square root of time. The reaction rate constants K=(square of the width of reaction layer / time) were evaluated. It was confirmed that the relation between K and the inverse of the temperature showed linearity above 773 K. (author)

Cermets based on rhenium and rare earth element oxides

International Nuclear Information System (INIS)

Varfolomeev, M.B.; Velichko, A.V.; Zajtseva, L.L.; Shishkov, N.V.

1977-01-01

The reduction of perrhenates of rare earth elements and of yttrium by hydrogen and the subsequent sintering have yielded cermets based on rhenium and rare earth element oxides inherent in which are more disperse and homogeneous structures than those of the ''molecular'' rare earth element-Tc cermets. The dispersity of cermets increases in the rare earth elements series from La to Lu. The microhardness of the Re phase in cermets is 490 kgf/mm 2 ; the total microhardness of a cermet is substantially higher

Micromagnetics of rare-earth efficient permanent magnets

Science.gov (United States)

Fischbacher, Johann; Kovacs, Alexander; Gusenbauer, Markus; Oezelt, Harald; Exl, Lukas; Bance, Simon; Schrefl, Thomas

2018-05-01

The development of permanent magnets containing less or no rare-earth elements is linked to profound knowledge of the coercivity mechanism. Prerequisites for a promising permanent magnet material are a high spontaneous magnetization and a sufficiently high magnetic anisotropy. In addition to the intrinsic magnetic properties the microstructure of the magnet plays a significant role in establishing coercivity. The influence of the microstructure on coercivity, remanence, and energy density product can be understood by using micromagnetic simulations. With advances in computer hardware and numerical methods, hysteresis curves of magnets can be computed quickly so that the simulations can readily provide guidance for the development of permanent magnets. The potential of rare-earth reduced and rare-earth free permanent magnets is investigated using micromagnetic simulations. The results show excellent hard magnetic properties can be achieved in grain boundary engineered NdFeB, rare-earth magnets with a ThMn12 structure, Co-based nano-wires, and L10-FeNi provided that the magnet’s microstructure is optimized.

The effect of hydrogen absorption on the structural, electronic and magnetic properties of the C15 Friauf-Laves phase compounds CeFe2, CeRu2 and LaRu2 : an x-ray absorption spectroscopy (XAS) study

International Nuclear Information System (INIS)

Chaboy, J.; Garcia, J.; Marcelli, A.

1995-08-01

An x-ray absorption spectroscopy (XAS) investigation of the structural changes occurred upon hydriding in the Friauf-Laves phase compounds CeFe 2 , CeRu 2 and LaRu 2 compounds is presented. The analysis of the extended x-ray absorption spectroscopy (EXAFS) spectra at the L-edges of the rare-earth and at the Fe K-edge indicates that the hydrogenation process leads to the suppression of the long-range crystalline order in all the hydride derivates investigated, as well as the different influence of H 2 in both the rare earth and transition metal sublattices. The correlation between the structural and magnetic changes induced by the hydrogen in the lost matrix is discussed in terms of the modification of the electronic properties, i.e., intermediate-valence of Ce, and of the hybridization between the transition metal and rare-earth

Research On Technology Of Making Rare Earth Alloy Having Rare Earth Content ≽30% From Ore (≽40% REO) Using Aluminum Thermal Technology In Arc Furnace

International Nuclear Information System (INIS)

Ngo Xuan Hung; Ngo Trong Hiep; Tran Duy Hai; Nguyen Huu Phuc

2014-01-01

Arc furnace was used to smelt materials consisting of rare earth ore having rare earth content of ≽40% REO, aluminum as the reducing agent and additives. Rare earth alloy was obtained with rare earth metal content of more than 30%. (author)

Rare earth industry in India

International Nuclear Information System (INIS)

Singh, D.S.

2016-01-01

Rare Earths (RE) comprises of 17 elements i.e. elements from atomic No. 57-71 (lanthanide series) along with yttrium (atomic No. 39) and scandium (atomic No. 21). They exhibit special electronic, magnetic, optical and catalytic properties. The first 7 elements in the lanthanide series from atomic Nos. 57 to 63 (La to Eu) are called Light Rare Earths (LRE), while the remaining elements from atomic Nos. 64 to 71 (Gd to Lu) are grouped as Heavy Rare Earths (HRE). Scandium and Yttrium have properties similar to HRE. The concentration of the REs in the earth's crust is as high as some other elements including that of copper. The only difference is that REs do not occur as separate minerals amenable for easy exploration and mining and are widely distributed across the earth's surface, hence they are called as REs. Resources In India, monazite has been the principal source of RE. It occurs in association with other heavy minerals, such as ilmenite, rutile, zircon etc. in the beach sands and inland placer deposits. The monazite content in this assemblage varies from negligible quantity to as high as 5%. As per AMD resource estimation, the reported resource of monazite in India is about 11.93 million tons which corresponds with about 6.9 million tons of RE oxides. Although India possesses large deposits of monazite, the heavier RE are not present in sufficient quantities in this mineral. (author)

Rare earth elements in a uranium deposit in Pedra, Pernambuco, Brazil

International Nuclear Information System (INIS)

Damascena, Kennedy Francys Rodrigues; Amaral, Romilton dos Santos; Santos Junior, Jose Araujo dos; Bezerra, Jairo Dias; Oliveira, Iane Andrade de; Silva, Alberto Antonio da

2013-01-01

Rare Earth Elements (REEs) are similar in the physical and chemical properties of their compounds and are most commonly found in nature associated with terrestrial radionuclides. The high interest in conducting research on REEs is due to their multiple applications and high economic value. In this light, the present study analyzed samples of soil and rocks from an anomalous area replete with uranium and thorium, in the town of Pedra, Pernambuco, Brazil, in an attempt to identify the occurrence and concentrations of these elements. For these analyses, neutron activation, followed by high-resolution gamma spectrometry, was used to define the REEs. The following REEs were identified in the study area: La, Ce, Nd, Sm, Eu, Tb, Yb, Lu, and Sc. The most abundant elements in the region, within samples of soil and rock, respectively, were: Ce (63-503 mg.kg -1 / 19.6 to 2243.5 mg.kg -1 ), Nd (25.0 to 249.0 mg.kg -1 / 3.8 to 1951.0 mg.kg -1 ), and La (30.6 to 253.0 mg.kg -1 / 12.1 to 517.0 mg.kg -1 ). The other REEs presented concentrations of between the detection limit and 46.0 mg.kg -1 . The results indicate that the Ce, La, and Nd concentrations appeared in up to 12 times the average occurrences in the earth's crust and up to 4.6 times higher than the averages reported in studies worldwide, including Brazil. Therefore, further studies are warranted to examine the economic viability of REEs in the area and to confirm the occurrence of these anomalous elements in the studied region. (author)

Determination of Barium and selected rare-earth elements in geological materials employing a HpGe detector by radioisotope excited x-ray fluorescence

International Nuclear Information System (INIS)

LaBrecque, J.J.; Preiss, I.L.

1984-01-01

The laterite material (geological) from Cerro Impacto was first studied by air radiometric techniques in the 1970's and was found to have an abnormally high radioactive background. Further studies showed this deposit to be rich in thorium, columbium, barium and rare-earth elements (mostly La, Ce, Pr and Nd). A similar work has been reported for the analysis of Brazil's lateritic material from Morro do Ferro to determine elemental compositions (including barium and rare-earth elements) and its relationship to the mobilization of thorium from the deposit using a Co-57 radioisotope source. The objective of this work was to develop an analytical method to determine barium and rare-earth element present in Venezuelan lateritic material from Cerro Impacto. We have employed a method before, employing a Si(Li) detector, but due to the low detection efficiencies in the rare-earth K-lines region (about 30 KeV - 40 KeV), we have decided to study the improvement in sensitivities and detection limits using an hyperpure germanium detector

Rare earth substitutional impurities in germanium: A hybrid density functional theory study

Science.gov (United States)

Igumbor, E.; Omotoso, E.; Tunhuma, S. M.; Danga, H. T.; Meyer, W. E.

2017-10-01

The Heyd, Scuseria, and Ernzerhof (HSE06) hybrid functional by means of density functional theory has been used to model the electronic and structural properties of rare earth (RE) substitutional impurities in germanium (REGe) . The formation and charge state transition energies for the REGe (RE = Ce, Pr, Er and Eu) were calculated. The energy of formation for the neutral charge state of the REGe lies between -0.14 and 3.13 eV. The formation energy result shows that the Pr dopant in Ge (PrGe) has the lowest formation energy of -0.14 eV, and is most energetically favourable under equilibrium conditions. The REGe induced charge state transition levels within the band gap of Ge. Shallow acceptor levels were induced by both the Eu (EuGe) and Pr (PrGe) dopants in Ge. The CeGe and ErGe exhibited properties of negative-U ordering with effective-U values of -0.85 and -1.07 eV, respectively.

Microstructural stability of heat-resistant high-pressure die-cast Mg-4Al-4Ce alloy

Energy Technology Data Exchange (ETDEWEB)

Wang, Wei; Zhang, Jinghuai; Li, Guoqiang; Feng, Yan; Su, Minliang; Wu, Ruizhi; Zhang, Zhongwu [Harbin Engineering Univ. (China). Key Laboratory of Superlight Material and Surface Technology; Jiao, Yufeng [Jiamusi Univ. (China). College of Materials Science and Engineering

2017-05-15

The thermal stability of Al-RE (rare earth) intermetallic phases with individual RE for heat-resistant high-pressure die-casting Mg-Al-RE alloys is investigated. The results of this study show that the main strengthening phase of Mg-4Al-4Ce alloy is Al{sub 11}Ce{sub 3}, whose content is about 5 wt.% according to quantitative X-ray diffraction phase analysis. The Al{sub 11}Ce{sub 3} phase appears to have high thermal stability at 200 C and 300 C, while phase morphology change with no phase structure transition could occur for Al{sub 11}Ce{sub 3} when the temperature reaches 400 C. Furthermore, besides the kinds of rare earths and temperature, stress is also an influencing factor in the microstructural stability of Mg-4Al-4Ce alloy.

Leaching of rare earth elements from bentonite clay

OpenAIRE

van der Watt, J.G; Waanders, F.B

2012-01-01

Due to increasing concerns of global rare earth element shortfalls in the near future, possible alternative sources of rare earth elements have recently become of economic interest. One such alternative is decanting acid mine water originating primarily from abandoned old mines in the Witwatersrand region of the Republic of South Africa. In this study, a novel way of rare earth element removal from the acid mine drainage was employed, making use of bentonite clay, which has very good adsorben...

Recovery of rare earths from red mud

International Nuclear Information System (INIS)

Bautista, R.G.

1992-01-01

The prospect for the recovery of rare earths from red mud, the bauxite tailings from the production of alumina is examined. The Jamaican red mud by far has the higher trace concentrations of lanthanum, cerium, neodymium, and yttrium. Scandium is also present. The dissolution of the rare earth is a major extraction problem because of the large volume of other materials. The recovery processes that have been proposed include the production of co-products such as iron, alumina, and titanium concentrates, with the rare earths going with the titanium. In this paper a critical examination of the possible processes are presented with the recommended research projects to be carried out

Radiological aspects in a monazite based rare earth production facility

International Nuclear Information System (INIS)

Harikumar, M.; Sujata, R.; Chinnaesakki, S.; Tripathi, R.M.; Puranik, V.D.; Nair, N.N.G.

2011-01-01

One of the largest reserves of monazite in the world is present in the Indian subcontinent. Monazite ore has around 8-9% thorium oxide and nearly 60% Rare earth oxides. Selective acid extraction is used to separate the composite rare earths. The main radiological hazard arises from the presence of thorium and its daughter products. Monitoring of the radiation field and air activity in the rare earths plant is done routinely to reduce the radiation exposure to plant personnel. The separation of uranium and rare earths from Thorium concentrate separated from Monazite is being done as a part of the THRUST (Thorium Retrieval, Recovery of Uranium and Re-storage of Thorium) project from 2004 at Indian Rare Earths Limited, Udyogamandal. The radiological aspect for this extraction of uranium and rare earths was studied. The general radiation field in the rare earth production plant was 0.3-5.0 μGyh -1 and the average short lived air activity was 46 ± 7 mWL. The long lived air activity arising from 232 Th is very insignificant radiologically. The occupational radiation exposure for the rare earths separation plant is only 6 % of the total dose and the estimated average individual dose is 1.6 mSv per year. Studies were also done to estimate the residual radioactivity in the separated rare earth compounds using gamma spectrometry and the results showed significant presence of 227 Ac arising due to the protactinium fraction in the thorium concentrate. This activity is not detectable in a freshly separated rare earth compound but can buildup with time. (author)

On solubility of rare earth chlorides in water at different temperatures

International Nuclear Information System (INIS)

Nikolaev, A.V.; Sorokina, A.A.; Sokolova, N.P.; Kotlyar-Shapirov, G.S.; Bagryantseva, L.I.

1978-01-01

Solubility of rare earth chlorides at -5, -10 and -15 deg C is studied. Rare earth chloride solubility dependences on the temperature in the interval from -15 to 50 deg C are presented. Decrease of solubility temperature coefficient to a zero is observed at temperature drop almost for all rare earth chlorides. Solubility temperature coefficient at the same temperature but for different rare earth chlorides reduces appreciably with the growth of rare earth chloride serial number. This testifies to the corresponding decrease of integral solution heat of rare earth chloride crystallohydrates

Rare earth elements and permanent magnets (invited)

Science.gov (United States)

Dent, Peter C.

2012-04-01

Rare earth (RE) magnets have become virtually indispensible in a wide variety of industries such as aerospace, automotive, electronics, medical, and military. RE elements are essential ingredients in these high performance magnets based on intermetallic compounds RECo5, RE2TM17 (TM: transition metal), and RE2TM14B. Rare earth magnets are known for their superior magnetic properties—high induction, and coercive force. These properties arise due to the extremely high magnetocrystalline anisotropy made possible by unique 3d-4f interactions between transition metals and rare earths. For more than 40 years, these magnets remain the number one choice in applications that require high magnetic fields in extreme operating conditions—high demagnetization forces and high temperature. EEC produces and specializes in RECo5 and RE2TM17 type sintered magnets. Samarium and gadolinium are key RE ingredients in the powder metallurgical magnet production processes which include melting, crushing, jet milling, pressing, sintering, and heat treating. The magnetic properties and applications of these magnets will be discussed. We will also briefly discuss the past, current, and future of the permanent magnet business. Currently, over 95% of all pure rare earth oxides are sourced from China, which currently controls the market. We will provide insights regarding current and potential new magnet technologies and designer choices, which may mitigate rare earth supply chain issues now and into the future.

Isopiestic determination of the activity coefficients of some aqueous rare earth electrolyte solutions at 250C. I. The rare earth chlorides

International Nuclear Information System (INIS)

Spedding, F.H.; Weber, H.O.; Saeger, V.W.; Petheram, H.H.; Rard, J.A.; Habenschuss, A.

1976-01-01

The osmotic coefficients of the aqueous trichlorides of La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y were determined from 0.1 M to saturation at 25 0 C. Semiempirical least-squares equations were obtained for the osmotic coefficients as a function of molality and these equations were used to calculate water activities and mean molal activity coefficients. The water activities of the light rare earth chlorides at constant molalities are higher than for the heavy rare earths, while the mean molal activity coefficients are larger for the heavy rare earths than for the light ones. The above effects are discussed in terms of changes in the cationic radii and hydration of the rare earth ions

Influence of Rare Earth Doping on the Structural and Catalytic Properties of Nanostructured Tin Oxide

Directory of Open Access Journals (Sweden)

Maciel Adeilton

2008-01-01

Full Text Available AbstractNanoparticles of tin oxide, doped with Ce and Y, were prepared using the polymeric precursor method. The structural variations of the tin oxide nanoparticles were characterized by means of nitrogen physisorption, carbon dioxide chemisorption, X-ray diffraction, and X-ray photoelectron spectroscopy. The synthesized samples, undoped and doped with the rare earths, were used to promote the ethanol steam reforming reaction. The SnO2-based nanoparticles were shown to be active catalysts for the ethanol steam reforming. The surface properties, such as surface area, basicity/base strength distribution, and catalytic activity/selectivity, were influenced by the rare earth doping of SnO2and also by the annealing temperatures. Doping led to chemical and micro-structural variations at the surface of the SnO2particles. Changes in the catalytic properties of the samples, such as selectivity toward ethylene, may be ascribed to different dopings and annealing temperatures.

Chlorination of UO2, PuO2, and rare-earth oxides using ZrCl4

International Nuclear Information System (INIS)

Sakamura, Yoshiharu; Inoue, Tadashi; Iwai, Takashi; Moriyama, Hirotake

2001-01-01

A new chlorination method using ZrCl 4 , which has a high reactivity with oxygen, has been investigated for more efficient oxide treatment. After actinide oxides are chlorinated and dissolved in a molten salt bath, actinide metals can be selectively collected using the electrorefining process. This process is well suited for pyrochemical reprocessing of metallic fuels. In LiCl-KCI eutectic melts, rare-earth oxides (Y 2 O 3 , La 2 O 3 , CeO 2 , and Nd 2 O 3 ) and actinide oxides (UO 2 and PuO 2 ) were chlorinated by adding ZrCl 4 . As a result, rare-earth and actinide elements were dissolved into the salt as trivalent ions and ZrO 2 was precipitated. When an excess of ZrCI 4 was added, oxides in powder form were completely chlorinated in five hours. It was demonstrated that the ZrCI 4 chlorination method, free from corrosive gas such as chlorine, was very simple and useful. (author)

Highly fractionated rare-earth elements in ferromagnesian chondrules from the Felix (CO3) meteorite

International Nuclear Information System (INIS)

Misawa, Keiji; Nakamura, Noboru

1988-01-01

Here we describe two ferromagnesian chondrules from the Felix (Ornans-subtype) carbonaceous chondrite which carry a marker signature of REE (rare earth element) fractionation in the nebula. Both show positive Ce and Yb anomalies and one exhibits a light/heavy REE fractionation. On the basis of the REE characteristics of these chondrules, as well as those of the authors' work on Allende (CV) [N Geochim. Cosmochim. Acta. in press], we suggest that one of the precursor materials of chondrules in CO-CV carbonaceous chondrites is a high-temperature condensate from the nebular gas. (author)

Rare earth elements in Japan Sea sediments and diagenetic behavior of Ce/Ce∗: results from ODP Leg 127

Science.gov (United States)

Murray, R.; Buchholtz ten Brink, Marilyn R.; Brumsack, Hans-Juergen; Gerlach, David C.; Russ III, G. Price

1991-01-01

The relative effects of paleoceanographic and paleogeographic variations, sediment lithology, and diagenetic processes on the recorded rare earth element (REE) chemistry of Japan Sea sediments are evaluated by investigating REE total abundances and relative fractionations in 59 samples from Ocean Drilling Program Leg 127.

China’s Rare Earths Production Forecasting and Sustainable Development Policy Implications

Directory of Open Access Journals (Sweden)

Xibo Wang

2017-06-01

Full Text Available Because of their unique physical and chemical properties, Rare earth elements (REEs perform important functions in our everyday lives, with use in a range of products. Recently, the study of China’s rare earth elements production has become a hot topic of worldwide interest, because of its dominant position in global rare earth elements supply, and an increasing demand for rare earth elements due to the constant use of rare earth elements in high-tech manufacturing industries. At the same time, as an exhaustible resource, the sustainable development of rare earth elements has received extensive attention. However, most of the study results are based on a qualitative analysis of rare earth elements distribution and production capacity, with few studies using quantitative modeling. To achieve reliable results with more factors being taken into consideration, this paper applies the generic multivariant system dynamics model to forecast China’s rare earth elements production trend and Hubbert peak, using Vensim software based on the Hubbert model. The results show that the peak of China’s rare earth elements production will appear by 2040, and that production will slowly decline afterwards. Based on the results, the paper proposes some policy recommendations for the sustainable development of China’s—and the world’s—rare earth elements market and rare earth-related industries.

Inverted opal luminescent Ce-doped silica glasses

Directory of Open Access Journals (Sweden)

R. Scotti

2006-01-01

Full Text Available Inverted opal Ce-doped silica glasses (Ce : Si molar ratio 1 ⋅ 10−3 were prepared by a sol-gel method using opals of latex microspheres as templates. The rare earth is homogeneously dispersed in silica host matrix, as evidenced by the absence of segregated CeO2, instead present in monolithic Ce-doped SG with the same cerium content. This suggests that the nanometric dimensions of bridges and junctions of the host matrix in the inverted opal structures favor the RE distribution avoiding the possible segregation of CeO2.

Mammography with rare earth intensifying screens

International Nuclear Information System (INIS)

Maurer, H.J.; Goos, F.

1987-01-01

Screens basing on rare earth phosphors with suitable films green or blue sensitive may be used in mammography with grids without diagnostic losses. Highest definition will be obtained with medium densities on film. High-speed screens may reduce dose, but definition is poor. Best compromise between speed and high definition may be reached with relative low thickness of phosphor layers. A system of high definition films (Medichrome) and special rare earth screens give best results. (orig.) [de

Determination of rare earth, major and trace elements in authigenic fraction of Andaman Sea (Northeastern Indian Ocean) sediments by inductively coupled plasma-mass spectrometry

Digital Repository Service at National Institute of Oceanography (India)

Alagarsamy, R.; You, C.-F.; Nath, B.N.; SijinKumar, A.V.

Downcore variation of rare earth elements (REEs) in the authigenic Fe-Mn oxides of a sediment core (covering a record of last approx. 40 kyr) from the Andaman Sea, a part of the Indian Ocean shows distinctive positive Ce and Eu anomalies...

On fluorozirconates and fluorohafnates of rare earths

International Nuclear Information System (INIS)

Korenev, Yu.M.; Antipov, P.I.; Novoselova, A.V.

1980-01-01

It has been shown by the method of X-ray phase analysis that on interaction between rare-earth fluorides and zirconium and hafnium tetrafluorides, compounds with 1:1, 1:2, 1:3 molar ratios of components are formed. Compounds of the LnHfF 4 type are prepared for all rare-earths. Fluoro-metals of the LnHf 2 F 11 composition are typical only of light lanthanides from lanthanum to neodymium, while pentafluorated salts Ln(EF 5 ) 3 are formed in the reaction between EF 4 with fluorides of heavy rare-earth elements from samarium to lutecium, as well as with yttrium trifluoride. Parameters of unit cells of heptafluohafnates and pentafluometallates are determined

Direct observation of multivalent states and 4 f →3 d charge transfer in Ce-doped yttrium iron garnet thin films

Science.gov (United States)

Vasili, H. B.; Casals, B.; Cichelero, R.; Macià, F.; Geshev, J.; Gargiani, P.; Valvidares, M.; Herrero-Martin, J.; Pellegrin, E.; Fontcuberta, J.; Herranz, G.

2017-07-01

Due to their large magneto-optic responses, rare-earth-doped yttrium iron garnets, Y3F e5O12 (YIG), are highly regarded for their potential in photonics and magnonics. Here, we consider the case of Ce-doped YIG (Ce-YIG) thin films, in which substitutional C e3 + ions are magnetic because of their 4 f1 ground state. In order to elucidate the impact of Ce substitution on the magnetization of YIG, we have carried out soft x-ray spectroscopy measurements on Ce-YIG films. In particular, we have used the element specificity of x-ray magnetic circular dichroism to extract the individual magnetization curves linked to Ce and Fe ions. Our results show that Ce doping triggers a selective charge transfer from Ce to the Fe tetrahedral sites in the YIG structure. This, in turn, causes a disruption of the electronic and magnetic properties of the parent compound, reducing the exchange coupling between the Ce and Fe magnetic moments and causing atypical magnetic behavior. Our work is relevant for understanding magnetism in rare-earth-doped YIG and, eventually, may enable a quantitative evaluation of the magneto-optical properties of rare-earth incorporation into YIG.

The preparation and corrosion resistance of Ce and Nd modified anodic films on aluminum

International Nuclear Information System (INIS)

Li Qizheng; Tang Yuming; Zuo Yu

2010-01-01

Rare earth element Ce and Nd modified anodic films were prepared on aluminum surface by a relatively simple method: the aluminum samples were first immersed in Ni(NO 3 ) 2 solutions containing Ce or Nd salts at 90 deg. C, then were dried and anodized. The contents of Ce or Nd in the anodic films were from 0.5% to 0.9%, and about 4-5% Ni was also introduced in the films. The modified anodic films were more compact with much smaller pores and increased hardness. In neutral, acidic and basic NaCl solutions, the rare earth modified films showed obviously improved corrosion resistance. The Ce modified films showed better corrosion resistance than Nd modified films. The cracking resistance of the films under heating was also improved.

High modulus rare earth and beryllium containing silicate glass compositions. [for glass reinforcing fibers

Science.gov (United States)

Bacon, J. F. (Inventor)

1976-01-01

Glass compositions having a Young's modulus of at least 16 million psi and a specific modulus of at least 110 million inches consisting essentially of approximately, by weight, 20 to 43% SiO2, 8 to 21% Al2O3, 4 to 10% BeO, 27 to 58% of at least one oxide selected from a first group consisting of Y2O3, La2O3, Nd2O3, Ce2O3, Ce2O3, and the mixed rare earth oxides, and 3 to 12% of at least one oxide selected from a second group consisting of MgO, ZrO2, ZnO and CaO are described. The molar ratio of BeO to the total content of the first group oxides is from 1.0 to 3.0.

Spectral determination of individual rare earths in different classes of inorganic compounds

International Nuclear Information System (INIS)

Karpenko, L.I.; Fadeeva, L.A.; Shevchenko, L.D.

1979-01-01

The conditions are found allowing to analyze various inorganic compounds for rare-earth elements without separation from non-rare-earth components. The influence of the plasma composition on the intensity of spectral lines of rare-earth elements is studied. The relative intensity of homologous spectral lines of various rare-earth elements remains constant regardless of the plasma composition. The conditions are found for the determination of individual rare-earth elements acting as both alloying additives (Csub(n) -- n x 10 -1 -n x 10 -3 %), and basic components (up to tens of per cent) in different classes of inorganic compounds of 1-7 elements. The general method is developed for the determination of individual rare-earth elements in mixtures of oxides of rare-earth elements, complex fluorides of rare-earth elements and elements of group 2, gallates, borates, germanates, vanadates of rare-earth elements and aluminium; zirconates-titanates of lead and barium, containing modifying additives of rare-earth elements, complex chalcogenides of rare-earth elements and elements of group 5

Heavy rare earths, permanent magnets, and renewable energies: An imminent crisis

International Nuclear Information System (INIS)

Smith Stegen, Karen

2015-01-01

This article sounds the alarm that a significant build-out of efficient lighting and renewable energy technologies may be endangered by shortages of rare earths and rare earth permanent magnets. At the moment, China is the predominant supplier of both and its recent rare earth industrial policies combined with its own growing demand for rare earths have caused widespread concern. To diversify supplies, new mining—outside of China—is needed. But what many observers of the “rare earth problem” overlook is that China also dominates in (1) the processing of rare earths, particularly the less abundant heavy rare earths, and (2) the supply chains for permanent magnets. Heavy rare earths and permanent magnets are critical for many renewable energy technologies, and it will require decades to develop new non-Chinese deposits, processing capacity, and supply chains. This article clarifies several misconceptions, evaluates frequently proposed solutions, and urges policy makers outside of China to undertake measures to avert a crisis, such as greater support for research and development and for the cultivation of intellectual capital. - Highlights: • Rare earths are needed for many efficient lighting and renewable energy technologies. • The industries for rare earths and permanent magnets are dominated by China. • China's reliability is compromised, necessitating non-Chinese mining and processing. • Recycling, substitution and reducing rare earth content are long-term solutions only. • Policy makers should support development of supply chains and intellectual capital

Micro-alloying Mg with Y, Ce, Gd and La for texture modification-A comparative study

International Nuclear Information System (INIS)

Stanford, N.

2010-01-01

A comparative study of the effectiveness of Y, La, Ce and Gd as texture modifiers during the extrusion of magnesium-based alloys has been carried out. It was found that La, Ce and Gd are all effective texture modifiers, being able to produce the 'rare earth' texture at the low alloying levels of 300, 400 and 600 ppm respectively. Y was not as effective as the other three elements in modifying the texture, and at no concentration studied did this element form a typical 'rare earth' texture. It is proposed that a strong interaction of solutes with dislocations and grain boundaries is responsible for the significant impact rare earth additions have on the extruded grain size and texture at very low alloying levels.

Handbook on the physics and chemistry of rare earths

International Nuclear Information System (INIS)

Gschneidner, K.A. Jr.; Eyring, L.

1982-01-01

This handbook is a six-volume work which covers the entire rare earth field in an integrated manner. Each chapter is a comprehensive, up-to-date, critical review of a particular segment of the field. The first volume is devoted to the rare earth metals, the second to rare earth alloys and intermetallics, and the third and fourth volumes to the non-metallic rare earth materials, including solutions, complexes and bioinorganic substances, in addition to solid inorganic compounds. The electronic structure of these unique elements is the primary basis of understanding their physical, metallurgical and chemical natures. The interrelationship of the 4f and valence electrons and the observed optical, electrical, magnetic, crystallographic, elastic, thermal, mechanical, chemical, geochemical and biological behaviors is brought forth time and again throughout the chapters. Also discussed are the preparative, separation and solution chemistry of the elements and their compounds and the various chemical and physical analytical methods for determining the rare earths in various materials and impurities in a rare earth matrix. Vol. 5 is a update complement of the previous volumes. Volume 6 is concerned with ternary and higher order materials. (Auth.)

Syntheses of rare-earth metal oxide nanotubes by the sol-gel method assisted with porous anodic aluminum oxide templates

International Nuclear Information System (INIS)

Kuang Qin; Lin Zhiwei; Lian Wei; Jiang Zhiyuan; Xie Zhaoxiong; Huang Rongbin; Zheng Lansun

2007-01-01

In this paper, we report a versatile synthetic method of ordered rare-earth metal (RE) oxide nanotubes. RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM, and X-ray diffraction (XRD) have been employed to characterize the morphology and composition of the as-prepared nanotubes. It is found that as-prepared RE oxides evolve into bamboo-like nanotubes and entirely hollow nanotubes. A new possible formation mechanism of RE oxide nanotubes in the AAO channels is proposed. These high-quantity RE oxide nanotubes are expected to have promising applications in many areas such as luminescent materials, catalysts, magnets, etc. - Graphical abstract: A versatile synthetic method for the preparation of ordered rare-earth (RE) oxide nanotubes is reported, by which RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates

Geochemistry of rare earths in main media of clay formation and sedimentation

International Nuclear Information System (INIS)

Bonnot-Courtois, C.

1981-01-01

This work aims i) at a better knowledge of rare earth behavior in surface conditions and ii) possible use of rare earth as a marker for argilaceous mineral genesis. Chemical properties of rare earths and geochemistry of these elements in main rocks are recalled. Rare earth behaviour during continental alteration process, experimental hydrolysis of various magmatic materials and rare earth geochemistry in argilaceous minerals in continental shelf are examined. Then some aspects of rare earth behaviour in oceans are studied: alteration of sea bed and hydrothermalism rare earth distribution in pelagic sediments red clays of deep seas and manganese nodules. In conclusion rare earth behaviour in sedimentary processes of the exogenous cycle is summarized [fr

Recycling of rare earths from Hg-containing fluorescent lamp scraps by solid state chlorination; Rueckgewinnung Seltener Erden aus quecksilberbelasteten Leuchtstoffen mittels Feststoffchlorierung

Energy Technology Data Exchange (ETDEWEB)

Lorenz, Tom; Froehlich, Peter; Bertau, Martin [TU Bergakademie Freiberg (Germany); Golon, Katja [FNE Entsorgungsdienste GmbH, Freiberg (Germany)

2015-10-15

Solid state chlorination with NH{sub 4}Cl comprises a method for rare earth recycling apart from pyro- or hydrometallurgical strategies. The examined partially Hg-containing fluorescent lamp scraps are rich in rare earths like La, Ce, Tb and Gd, but especially in Y and Eu. By mixing with NH{sub 4}Cl and heating up to NH{sub 4}Cl decomposition temperature in a sublimation reactor, Y and Eu could be transferred selectively into their respective metal chlorides with high yields. The yield and selectivity depend on temperature and the ratio of NH{sub 4}Cl to fluorescent lamp scraps, which were varied systematically.

Determination of rare earth contents in plant and soil by neutron activation analysis (NAA)

International Nuclear Information System (INIS)

Krafka, B.; Lin, X.L.; Henkelmann, R.

1998-01-01

Full text: The results presented are typical analytical results for Bavarian soils and plants. Plants and soils collected from identical sites are used to quantify the ratios of rare earth contents. This work has been in close cooperation with several governmental institutions, who are responsible for the protection and surveillance of agricultural sites and wooded areas. Routine sampling takes place on selected areas in the federal state of Bavaria, and the samples (soil and plants as wheat, corn or needles) are analysed with use of AAS, ICP-OES or ICP-MS techniques. INAA as an alternative method is in this context very interesting because it does not involve any sample pretreatment, prior to irradiation. It could be shown for chosen elements (K, Cr, Zn etc.), that incomplete digestion can lead to results which are remarkably lower than the total content in the sample. INAA also is an excellent technique to analyse rare earth elements. The advantage of analysing the original material, which only needs to be dried and homogenized, allows the determination of total values for most of the elements, independent of the chemical binding state of the atoms. Due to this reason, INAA is often called 'independent of matrix'. Only when the g-spectroscopy after activation is carried out, the main components may disturb the determination of trace elements. In soils, the matrix allows the pure instrumental determination of 9 rare earth elements (Ce, Dy, Eu, La, Lu, Nd, Sm, Tb, Yb). In plant material, the rare earth concentrations are much lower, so a chemical separation is needed in order to remove or reduce the main interferences like Na, K, Br etc. This combination of NAA with radiochemical separation is called Radiochemical Neutron Activation Analysis (RNAA) and allows to determine the same elements as in soils, except Dy

Corrosion Resistance of Murataite-Based Ceramics Containing Simulated Actinide/Rare Earth Fraction of High Level Waste

International Nuclear Information System (INIS)

Stefanovsky, S.V.; Varlakova, G.A.; Burlaka, O.A.; Stefanovsky, O.I.; Nikonov, B.S.; Yudintsev, S.V.

2009-01-01

Two samples of murataite-based ceramics containing simulated Actinide/Rare Earth (An/RE) fraction of high level waste (HLW) produced by a cold crucible inductive melting (CCIM) were tested using a single-pass-flow-through (SPFT) procedure. As-prepared and leached samples were examined by X-ray diffraction (XRD) and scanning electron microscopy with energy dispersive system (SEM/EDS). The as-prepared ceramics were composed of murataite, perovskite and crichtonite as well as minor zirconolite and rutile (in one sample). Elemental concentrations at pH=2 and T=90 deg. C were measured and leach rates were calculated. Perovskite concentrating Ca and Ce-group REs (La, Ce, Pr, Nd) was found to be the lowest durable phase. Leach rates of Ca and Ce-group REs (Ce, Nd) from the sample with higher perovskite content were found to be higher than those of U and Zr by one to three orders of magnitude. Elemental leach rates from the ceramic with lower perovskite content are lower by up to 10 times. (authors)

PROCESS FOR SEPARATING AMERICIUM AND CURIUM FROM RARE EARTH ELEMENTS

Science.gov (United States)

Baybarz, R.D.; Lloyd, M.H.

1963-02-26

This invention relates to methods of separating americium and curium values from rare earth values. In accordance with the invention americium, curium, and rare earth values are sorbed on an anion exchange resin. A major portion of the rare earth values are selectively stripped from the resin with a concentrated aqueous solution of lithium chloride, and americium, curium, and a minor portion of rare earth values are then stripped from the resin with a dilute aqueous solution of lithium chloride. The americium and curium values are further purified by increasing the concentration of lithium chloride in the solution to at least 8 molar and selectively extracting rare earth values from the resulting solution with a monoalkylphosphoric acid. (AEC)

Environmental aspects in the processing of rare earth ores and minerals

International Nuclear Information System (INIS)

Bhattacharya, R.

2011-01-01

In India, rare earths are extracted from the mineral monazite which occurs abundantly along with other heavy minerals in the coastal beach sands. Monazite, apart from rare earths, also contains uranium and thorium. Rare earths can be obtained from monazite either by acid digestion route or by alkaline digestion route. In India, although pilot scale studies have been carried out extraction of rare earths by acid digestion route, however, alkali digestion route has been predominantly followed for commercial extraction of rare earths

Squeezing clathrate cages to host trivalent rare-earth guests

Energy Technology Data Exchange (ETDEWEB)

Wang, Jian [Iowa State Univ., Ames, IA (United States). Department of Chemistry; Ames Lab., Ames, IA (United States); He, Yuping [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Mordvinova, Natalia E. [Laboratoire CRISMAT, ENSICAEN, CNRS UMR (France); Lebedev, Oleg [Laboratoire CRISMAT, ENSICAEN, CNRS UMR (France); Kovnir, Kirill [Iowa State Univ., Ames, IA (United States). Department of Chemistry; Ames Lab., Ames, IA (United States)

2017-11-01

Strike difference of the trivalent rare-earth cations from their alkali and alkaline-earth peers is in the presence of localized 4f-electrons and strong spin-orbit coupling. Placing trivalent rare-earth cations inside the fullerene molecules or in between the blocks of itinerant magnetic intermetallics gave rise to plethora of fascinating properties and materials. A long-time missing but hardly desired piece is the semiconducting or metallic compound where rare-earth cations are situated inside the oversized polyhedral cages of three-dimensional framework. In this work we present a synthesis of such compounds, rare-earth containing clathrates Ba_8-xR_xCu₁₆P₃₀. The unambiguous proofs of their composition and crystal structure were achieved by a combination of synchrotron powder diffraction, time-of-flight neutron powder diffraction, scanning-transmission electron microscopy, and electron energy-loss spectroscopy. Our quantum-mechanical calculations and experimental characterizations show that the incorporation of the rare-earth cations significantly enhances the hole mobility and concentration which results in the drastic increase in the thermoelectric performance.

Rare earths: harvesting basic research for technology

International Nuclear Information System (INIS)

Jagatap, B.N.

2014-01-01

In recent years, rare earths are increasingly becoming a versatile platform for basic research that presents enormous technological potentials. A variety of nano-sized inorganic matrices varying from oxides, phosphates, gallates and aluminates, tungstates, stannates, vanadates to fluorides doped with different lanthanide ions have been synthesized and their optical properties have been investigated in the Chemistry Group, BARC. Another interesting application is laser cooling of solids using rare earth doped glasses with potential applications in remote cooling of electronic devices. Combining the luminescence properties of rare earths with photonic crystals is yet another potent area with wide ranging applications. In this presentation we provide an overview of these developments with examples from the R and D programs of the Chemistry Group, BARC

Contributions to the rare earths to science and technology

International Nuclear Information System (INIS)

Spedding, F.H.

1975-01-01

This is a brief summary of some areas of science where the rare earths have already played an important role and of other areas where they are almost certain to be helpful. The discovery, abundance, separation, and properties of rare earths are discussed. It is pointed out that the rare earths comprise almost one-fourth of the known metals, and their alloys a third of the possible alloys

Separation of rare earths by liquid-liquid extraction

International Nuclear Information System (INIS)

Helgorsky, M.; Leveque, M.

1978-01-01

The elements of the rare earth family are characterised by very similar chemical properties connected with their special electronic structure. The purification of the rare earths sold by RHONE-POULENC is now done by the liquid-liquid extraction technique. The development of different extracting agents and also counter-current techniques have led to solvent extraction replacing the other fractionation techniques because of its efficiency and low cost. There are usually several possible solutions to the main problem of choosing the extracting agent and its mode of use. The difficulty is to find the most economical one taking account of the thermodynamic and hydrodynamic constraints of the solvent. It is shown how ideas about the separation have changed over the course of the development of the uses of the rare earths, ending finally in an integrated scheme that makes RHONE-POULENC a world leader of manufacturers of separated rare earths [fr

Rare-earth metal prices in the USA ca. 1960 to 1994

Science.gov (United States)

Hedrick, James B.

1997-01-01

Rare-earth metal prices were compiled from the late 1950s and early 1960s through 1994. Although commercial demand for rare-earth metals began in 1908, as the alloy mischmetal, commercial quantities of a wide range of individual rare-earth metals were not available until the late 1950s. The discovery of a large, high-grade rare-earth deposit at Mountain Pass. CA, USA, in 1949, was significant because it led to the production of commercial quantities or rare-earth elements that reduced prices and encouraged wider application of the materials. The availability of ore from Mountain Pass, and other large rare-earth deposits, especially those in Australia and China, has provided the world with abundant resources for rare-earth metal production. This availability, coupled with improved technology from Government and private-sector metallurgical research, has resulted in substantial decreases in rare-earth metal prices since the late 1950s and early 1960s. Price series for the individual rare-earth metals (except promethium) are quoted on a kilogram basis from the late 1950s and early 1960s through 1994. Prices are given in US dollars on an actual and constant dollar basis. Industrial and economic factors affecting prices during this time period are examined.

A survey of 16 rare Earth elements in the major foods in China.

Science.gov (United States)

Jiang, Ding Guo; Yang, Jie; Zhang, Shuo; Yang, Da Jin

2012-06-01

The aim of this survey was to investigate the level of contamination of the most consumed foods in China with 16 rare earth elements (REEs), and to provide the basic data for establishing and revising food safety standards for REEs. Sixteen REEs in foods were measured by inductively coupled plasma-mass spectrometry (ICP-MS) in the labs of the Centers for Disease Control and Prevention of four provinces and two municipalities, during 2009-2010. 1 231 samples were analyzed and 19 121 concentration data of 16 REEs were collected. The REEs levels in the investigated foods varied significantly. The concentrations of cerium (Ce), dysprosium (Dy), yttrium (Y), lanthanum (La), and neodymium (Nd) were relatively high, while the remaining eleven REEs were at low levels. The mean values of total rare earth element oxides (REOs) in cereals, fresh vegetables, fresh aquatic products, fresh meats and eggs varied from 0.052 mg/kg to 0.337 mg/kg. 16 REEs in the major foods were at very low contamination levels in the investigated regions. Copyright © 2012 The Editorial Board of Biomedical and Environmental Sciences. Published by Elsevier B.V. All rights reserved.

X-ray absorption experiments on rare earth and uranium compounds under high pressure

International Nuclear Information System (INIS)

Schmiester, G.

1987-01-01

After an introduction into the phenomenon of the mixed valency and the method of measuring the microstructures by X-ray absorption spectroscopy in the area of the L edges under pressure, the results of investigations at selected substitutes of the chalcogenides and puictides of the rare earths and the uranium were given. Thus, pressure-induced valency transitions in YbS and YbTe, instabilities in valency and structural phase transitions in EUS and SmTe as well as the change in the electron structure in USb under pressure were investigated in order to answer questions of solid state physics (e.g. semiconductor-metal transitions, correlation between valency and structural phase transitions). Hybridization effects in L III spectra of formally tetravalent Ca are analyzed at CeF 4 and CeO 2 (insulators) and the role of final state effects in the L III spectra are analyzed at EuP 2 P 2 and TmSe-TmTe (semiconductor systems). (RB) [de

Rare earths: critical elements for various applications and challenges in their separation

International Nuclear Information System (INIS)

Singh, D.K.; Chakravartty, J.K.

2015-01-01

High purity rare earths oxides, metal and alloys find wide applications in high tech area such as nuclear energy, permanent magnets, materials for storing hydrogen, phosphors, laser, etc. Rare earths consists a group of 15 elements from La to Lu in the periodic table and it also includes Sc and Y. Due to similar chemical nature owing to common oxidation state of +3, rare earths are very difficult to separate from each other. They have very low separation factors with acidic extractants like D2EHPA and EHEHPA and hence require large number of stages in various cascade of extraction process. Monazite (a source of rare earths, thorium and uranium) is processed at IREL to separate rare earths from thorium and uranium. The rare earths are fractionated into three groups namely light rare earths (LRE), middle rare earths (MRE) and heavy rare earths (HRE) by solvent extraction method employing EHEHPA as extractant

Study of the oxygen reduction reaction using Pt-Rare earths (La, Ce, Er) electrocatalysts for application of PEM fuel cells; Estudo da reacao de reducao do oxigenio utilizando eletrocatalisadores a base de Pt-terras raras (La, Ce, Er) para aplicacao em celulas a combustivel tipo PEM

Energy Technology Data Exchange (ETDEWEB)

Gomes, Thiago Bueno

2013-07-01

The complexity of the oxygen reduction reaction (ORR) and its potential losses make it responsible for the most part of efficiency losses at the Fuel Cells. For this reaction the electrocatalyst witch is most appropriated and shows better performance is platinum, a noble metal that elevates the cost, raising barriers for Fuel Cells technology to enter the market. First this work focuses on reducing the amount of platinum used in the cathode, by being replaced by rare earths. The most common methods of synthesis involves a large amount of steps and this work proposed to prepare the electrocatalyst through a simpler way that would not take so many steps and time to be done. Using an ultrasound mixer the electrocatalyst was prepared mixing platinum supported on carbon black and the rare earths lanthanum, cerium and erbium oxides to be applied in a half-cell study of the ORR. The Koutecky-Levich plots shows that among the electrocatalysts prepared the Pt80Ce20/C had the catalytic activity close to the commercial BASF platinum on carbon black, suggesting that the reaction was taken by the 4-electron path. As found in some works in literature, among the rare earth used to study the ORR, cerium is the one witch shows the better performance because it is able to store and provide oxygen. This feature is of great interest for the ORR because this reaction is first order to the oxygen concentration. Results show that is possible to reduce the amount of platinum maintaining the same electrocatalyst activity. (author)

Preliminary geological assessment for rare earths at Ombo Area, San Vicente, Northern Palawan

International Nuclear Information System (INIS)

Ramos, Angelito F.; Santos, Gabriel Jr.; Magsambol, Wilfred N.; Castillo, Marilyn K.; Tabora, Estrelita U.

2001-04-01

A preliminary geological assessment for rare earths was conducted along Ombo beach area, San Vicente, northern Palawan to evaluate the potential geologic reserve and to determine the relative concentration of REE, thorium and uranium. This investigation also aims to establish the distribution of heavy minerals. The study area, covering, about 6500 m 2 is comprised of the undisturbed beach sand deposits confined between the high tide line and the base of the mountains that borders the coastline. The investigation involved the establishment of shallow test pits with depths varying from one meter ot less than three meters. A total of 23 heavy mineral panned concentrates were collected. All the samples were analyzed for REE, Th and U using the portable X-MET 820 x-ray fluorescence and GR-320 gamma ray spectrometer. Radiometric measurements were also taken along the stretch of Ombo beach to establish the natural background radioactivity. The radiometric values vary from 27 cps to 420 cps. The high readings could be attributed to the presence of radioactive rare earth bearing minerals, principally allanite. This initial investigation indicates a positive geologic reserve of approximately 19,000 metric tons beach sand deposits, containing an average grade of 22.19% REE (Ce, La), 0.85% Th and 0.55% U. The average distribution of heavy minerals is 3600 gm heavies per cubic meter. Moreover, a probable geologic reserve of about 41,000 metric tons with an average grade of 22.13% REE (Ce, La), 0.85% Th and 0.55% U was also determined. The average distribution of heavy minerals is about 3300 gm heavies per cubic meter. (Author)

A Study on Electrochemical Reduction of Rare Earth Oxides in Molten LiCl-Li{sub 2}O Salt

Energy Technology Data Exchange (ETDEWEB)

Lee, Min Woo; Jeong, Sang Mun; Lee, See Hoon [Chungbook National University, Chungju (Korea, Republic of); Sohn, Jung Min [Chonbuk National University, Jeonju (Korea, Republic of)

2016-05-15

In this study, the electrochemical reduction of RE{sub 2}O{sub 3} (RE = Nd or Ce) has been conducted via co-reduction NiO to increase the reduction degree of the rare earth oxides in molten molten LiCl containing 1wt% Li{sub 2}O. The electrochemical reduction behavior of the mixed RE{sub 2}O{sub 3}-NiO oxide has been investigated and the reduction path of RE{sub 2}O{sub 3} has been proposed. An electorchemical spent fuel processing technology, pyroprocessing, has been developed for recycling of spent fuel to be applied to a sodium-cooled fast reactor. The spent fuel is reduced in the oxide reduction process. It is well known that the rare earth oxides are hardly reduced due to their electrochemical and thermodynamic stability. The rare earth oxides unreduced in the reduction process can cause problems via reaction with UCl{sub 3} in the electrorefiner. To tackle those problems, the electrochemical reduction of rare earth oxide has been conducted via co-reduction of NiO in LiCl molten salt containing 1 wt% Li{sub 2}O. The reduction of the oxide mixture starts from the reduction of NiO to Ni, followed by that of RE{sub 2}O{sub 3} on the produced Ni to form intermetallic RENi{sub 5}. The mixed oxide pellets were successfully reduced to the RENi5 alloy by constant electrolysis at 3.0 V at 650 .deg. C. The crucial aspect to these results is that the thermodynamically stable rare-earth oxide, Nd{sub 2}O{sub 3} was successfully converted to the metal in the presence of NiO.

Coprecipitation of rare earth elements with hydroxyapatite

International Nuclear Information System (INIS)

Fujino, Osamu

1979-01-01

The distribution behavior of trace rare earth elements between an aqueous phase and hydroxyapatite crystals was investigated. The apatite prepared by adding phosphate ion extremely slowly to an aqueous solution containing calcium, rare earth elements, ethylenediamine and nitrilotriacetate ion at 80 0 C. Apparently the coprecipitation reaction seems to be anomalous, because the apparent distribution coefficient did not have a constant value through the reaction. But when the true distribution coefficient was calculated by using the thermodynamic data at 80 0 C, it was revealed that rare earth ions were coprecipitated obeying logarithmic distribution law. The true distribution coefficient values of trivalent yttrium, scandium, europium and cerium ions were about 10sup(7.3), 10sup(9.8), 10sup(7.4) and 10sup(6.5) respectively. (author)

Thermodynamic Considerations of Direct Oxygen Removal from Titanium by Utilizing the Deoxidation Capability of Rare Earth Metals

Science.gov (United States)

Okabe, Toru H.; Zheng, Chenyi; Taninouchi, Yu-ki

2018-06-01

Oxygen removal from metallic Ti is extremely difficult and, currently, there is no commercial process for effectively deoxidizing Ti or its alloys. The oxygen concentration in Ti scraps is normally higher than that in virgin metals such as in Ti sponges produced by the Kroll process. When scraps are remelted with virgin metals for producing primary ingots of Ti or its alloys, the amount of scrap that can be used is limited owing to the accumulation of oxygen impurities. Future demands of an increase in Ti production and of mitigating environmental impacts require that the amount of scrap recycled as a feed material of Ti ingots should also increase. Therefore, it is important to develop methods for removing oxygen directly from Ti scraps. In this study, we evaluated the deoxidation limit for β-Ti using Y or light rare earth metals (La, Ce, Pr, or Nd) as a deoxidant. Thermodynamic considerations suggest that extra-low-oxygen Ti, with an oxygen concentration of 100 mass ppm or less can be obtained using a molten salt equilibrating with rare earth metals. The results presented herein also indicate that methods based on molten salt electrolysis for producing rare earth metals can be utilized for effectively and directly deoxidizing Ti scraps.

Rare earths refining by vacuum sublimation method

International Nuclear Information System (INIS)

Rytus, N.N.

1983-01-01

The process of rare earths refining by the sUblimation; method in high and superhigh oil-free vacuum, is investigated. The method is effective for rare earths obtaining and permits to prepare metal samples with a high value of electric resistance ratio γ=RsUb(298 K)/Rsub(4.2 K). The estimation of general purity is performed for Sm, Eu, Yb, Tm, Dy, Ho, Er and Se

Immobilization of Radioactive Rare Earth oxide Waste by Solid Phase Sintering

International Nuclear Information System (INIS)

Ahn, Byung Gil; Park, Hwan Seo; Kim, Hwan Young; Lee, Han Soo; Kim, In Tae

2010-01-01

In the pyroprocessing of spent nuclear fuels, LiCl-KCl waste salt containing radioactive rare earth chlorides are generated. The radioactive rare earth oxides are recovered by co-oxidative precipitation of rare earth elements. The powder phase of rare earth oxide waste must be immobilized to produce a monolithic wasteform suitable for storage and ultimate disposal. The immobilization of these waste developed in this study involves a solid state sintering of the waste with host borosilicate glass and zinc titanate based ceramic matrix (ZIT). And the rare-earth monazite which synthesised by reaction of ammonium di-hydrogen phosphate with the rare earth oxides waste, were immobilized with the borosilicate glass. It is shown that the developed ZIT ceramic wasteform is highly resistant the leaching process, high density and thermal conductivity.

Several new phases in RE-Mg-Ge systems (RE = rare earth metal) - syntheses, structures, and chemical bonding

International Nuclear Information System (INIS)

Suen, Nian-Tzu; Bobev, Svilen

2012-01-01

Reported are the synthesis and structural characterization of Ce_5Mg_8Ge_8 (its own structure type), CeMg_2_-_xGe_2_+_x (BaAl_4-type structure), RE_4Mg_7Ge_6 (RE = Ce-Nd, Sm; La_4Mg_7Ge_6-type structure), and RE_4Mg_5Ge_6 (RE = Ce, Pr; Tm_4Zn_5Ge_6-type structure). The structures of these compounds have been established by single-crystal and powder X-ray diffraction. These compounds are closely related to each other not only in their chemical compositions but also in their structures. A common structural feature of all are MgGe_4 tetrahedra, which are connected by corner- and/or edge-sharing into complex polyanionic frameworks with the rare-earth metal atoms filling the ''empty'' space. The structures are compared to known types of structures, and we have investigated the chemical bonding in Ce_5Mg_8Ge_8 with electronic structure calculations, which were carried out by the tight-bonding linear muffin-tin orbital (TB-LMTO) method. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Loparite-(Ce) from the Khibiny Alkaline Pluton, Kola Peninsula, Russia

Science.gov (United States)

Konopleva, N. G.; Ivanyuk, G. Yu.; Pakhomovsky, Ya. A.; Yakovenchuk, V. N.; Mikhailova, Yu. A.

2017-12-01

Data on the occurrence, morphology, anatomy, composition, and formation conditions of loparite-(Ce) in the Khibiny alkaline pluton are given. Loparite-(Ce), (Na,Ce,Sr)(Ce,Th)(Ti,Nb)2O6, resulted from metasomatic alteration and assimilation of metamorphic host rocks at the contact with foyaite as well as foyaite on the contact with foidolite. This alteration was the highest in pegmatite, and albitite developed there. A decrease in temperature resulted in enrichment of the perovskite and tausonite endmembers in loparite-(Ce) owing to a decrease in the loparite and lueshite endmembers. La and Ce sharply predominate among rare earth elements in the composition of loparite-(Ce).

Crystalline and amorphous rare-earth metallic compounds

International Nuclear Information System (INIS)

Burzo, E.

1975-01-01

During the last years the study of magnetic behaviour of rare-earth (or yttrium) compounds with cobalt and iron has growth of interest. This interest of justified by a large area of experimental and theoretical problems coming into being in the study of some rare-earth materials as well as in their technical applications. In the last three years a great number of new rare earth materials were studied and also new models explaining the magnetic behaviour of these systems have been used. In this paper we refer especially to some typical systems in order to analyse the magnetic behaviour of iron and cobalt and also the part played by the magnetic interactions in the values of the cobalt or iron moments. The model used will be generally the molecular field model. In the second chapter we present comparatively the structure of crystalline and amorphous compounds for further correlation with the magnetic properties. In chapter III we analyse the magnetic interactions in some crystalline and amorphous rare-earth alloys. Finally, we exemplify the ways in which we ensure better requried characteristics by the technical utilizations of these materials. These have in view the modifications of the magnetic interactions and are closely related with the analysis made in chapter III

Rare earth point defects in GaN

Energy Technology Data Exchange (ETDEWEB)

Sanna, S.

2007-12-14

In this work we investigate rare earth doped GaN, by means of theoretical simulations. The huge unit cells necessary to model the experimental system, where dilute amount of rare earth ions are used, are handled with the charge self consistent density-functional based-tight binding (SCC-DFTB) calculational scheme. The method has been extended to include LDA+U and simplified self interaction corrected (SIC)-like potentials for the simulation of systems with localised and strongly correlated electrons. A set of tight-binding parameters has been created to model the interaction of GaN with some dopants, including a selection of lanthanide ions interesting due to their optical or magnetic properties (Pr, Eu, Gd, Er and Tm). The f-electrons were treated as valence electrons. A qualitatively correct description of the band gap is crucial for the simulation of rare earth doped GaN, because the luminescence intensity of the implanted samples depends on the size of the host band gap and because the rare earths could introduce charge transition levels near the conduction band. In this work these levels are calculated with the Slater-Janak (SJ) transition state model, which allows an approximate calculation of the charge transition levels by analysing the Kohn-Sham eigenvalues of the DFT. (orig.)

Rare earth element abundances and distribution patterns in plant materials

International Nuclear Information System (INIS)

Aidid, S.B.

1994-01-01

Eight out of the fourteen rare earth elements were estimated from the leaves of Pelthophorum pterocarpum, the leaves and roots of Impatiens balsamina, and the soils from four sampling sites by instrumental neutron activation analysis. The chondrite normalized rare earth element abundances and distribution patterns in the plant materials were found to be significantly correlated to the abundances of the rare earth elements occurring in the soils. The extent of accumulation of the rare earth elements in some plant materials was also governed by the age of the plants and the plant organs. (author) 16 refs.; 4 figs.; 3 tabs

Magnetic rare earth superlattices

DEFF Research Database (Denmark)

Majkrzak, C.F.; Kwo, J.; Hong, M.

1991-01-01

Advances in molecular beam epitaxy deposition techniques have recently made it possible to grow, an atomic plane at a time, single crystalline superlattices composed of alternating layers of a magnetic rare earth, such as Gd, Dy, Ho, or Er, and metallic Y, which has an identical chemical structure...

Solvent Extraction of Rare Earths by Di-2 Ethylhexyl Phosphoric Acid

International Nuclear Information System (INIS)

Srinuttrakul, Wannee; Kranlert, Kannika; Kraikaew, Jarunee; Pongpansook, Surasak; Chayavadhanangkur, Chavalek; Kranlert, Kannika

2004-10-01

Solvent extraction has been widely applied for individual rare earth separation because the separation time is rapid and a large quantity of products is obtained. In this work, this technique was utilized to extract mixed rare earths, obtained from monazite digestion process. Di-2-ethylhexyl phosphoric acid (D2EHPA) was used as an extractant. The factors affected the extraction including HNO 3 concentration in mixed rare earth nitrate solution and the amount of D2EHPA were studied. The appropriate concentrations of HNO 3 and D2EHPA were found to be 0.01 and 1.5 M, respectively. From the result of equilibrium curve study, it was observed that heavy rare earths were extracted more efficient than light rare earths. A 6-stage continuous countercurrent solvent extraction was simulated for rare earth extraction. The optimum ratio of solvent to feed solution (S/F) was 2. Because of the high cost of D2EHPA, 1.0 M of D2EHPA was suitable for the rare earth extraction by the continuous countercurrent solvent extraction

The electrodeposition and rare earths reduction in the molten salt actinides recovery systems using liquid metal

International Nuclear Information System (INIS)

Shim, J-B.; Lee, J-H.; Kwon, S-W.; Ahn, B-G.; Woo, M-S.; Lee, B-J.; Kim, E-H.; Park, H-S.; Yoo, J-H.

2005-01-01

A pyrochemical partitioning system uses liquid metals such as cadmium and bismuth in order to recover the actinide metals from a molten salt mixture containing rare earth fission product metals. The liquid metals play roles as a cathode in the electrowinning or an extracting phase in the reductive extraction operation. The product resulting from the above operations is metal-cadmium or-bismuth alloy, which should contain the rare earth element amounts as low as possible for a transmutation purpose. In this study, the electrodeposition behaviours of uranium and lanthanide elements such as La, Ce and Nd were investigated for solid molybdenum and liquid cadmium electrodes in a molten LiCl-KCl eutectic salt. Electrochemical methods used are a cyclic voltammetry (CV) and a chronopotentiometry for monitoring the salt phase and recovering the metals, respectively. The CV graphs for monitoring the oxidizing agent CdCl 2 in the salt phase were obtained. These show a time dependently disappearance of the oxidizing agent corresponding to the formation of UCl 3 by inserting the uranium metal into the salt. Also, a sequential oxidation technique which is added at a controlled amount of the oxidizing agents into the salt phase was applied. It was found that this method is feasible for the selective reduction of the rare earths content in liquid metal alloys. (author)

Extraction-differential-photometric method to determine rare earths of cerium subgroup

International Nuclear Information System (INIS)

Askerov, D.N.; Gusejnov, I.K.; Melikov, A.A.

1985-01-01

The extraction - photometric method to determine great quantities of rare earths of the cerium subgroup as a complex with antipyrine A and diphenylguanidine is developed. Isobutyl and n-butyl alcohols are used as extractants. It is established that proportional dependence between relative optical density and concentration of rare earths of the cerium subgroup in the solution takes place in the concentration interval of 10.3-14.7 μg of rare earths in 1 ml of the solution. Determination error is+-1.12%. The technique is used to determine rare earths of the cerium subgroup in rare earth oxides of a mixed composition, as well as in monozite and loparite

2004 Top 10 Chinese Rare Earth Events

Institute of Scientific and Technical Information of China (English)

无

2005-01-01

1. Management to the Investment in Rare Earth IndustryConfirmedIn July 2004, "Decision on the Reform in Investment System" was formally publicized by the State Council of the People's Republic of China. The fifth item in the Decision stipulates that ore exploitation, smelting & separation and rare earth deep-processed projects with total investment over RMB￥100 million should be approved by the investment governing department of the State Council, and that other

ELECTRICAL PROPERTIES OF COMPOUNDS AND ALLOYS OF RARE-EARTH METALS WITH ELEMENTS OF GROUPS V AND VI

Energy Technology Data Exchange (ETDEWEB)

Reid, F. J.; Matson, L. K.; Miller, J. F.; Himes, R. C.

1963-04-15

The electric properties of rare earth compounds and alloys with As, Sb, Se, and Te are reported. Without exception, samples of Se and Te compounds with normally trivalent Nd, Gd, and Ce having synthetic compositions, MX and M/sub 3/X/ sub 4/, are n-type wrth free electron concentrations in the range 10/sup 20/ to 10 /sup 22//cm/sup 3/, and have very low electric resistivities. Room temperature electric properties and thermoelectric data are tabulated. (P.C H.)

Ln3+ (Ln=Ce, Tb, Dy) and Hf doping of LuI3 powders – A material and spectroscopic study

International Nuclear Information System (INIS)

Wiatrowska, Aneta; Keur, Wilco; Ronda, Cees

2016-01-01

The moisture sensitivity of LuI 3 :Ce,Hf and luminescent properties of undoped LuI 3 and LuI 3 :M (M=Ce 3+ , Tb 3+ , Dy 3+ ) powders were investigated. The possibility of improving the air and moisture stability of LuI 3 :Ce by Hf doping was tested. It was proven that the Hf contribution to the LuI 3 :Ce stability is very limited and is insignificant to render LuI 3 :Ce scintillator powders suitable for applications. Photoluminescence results of LuI 3 without dopants added on purpose showed luminescence due to a plurality of rare-earth elements' impurities. Two types of self-trapped luminescence were found. Energy transfer between host lattice, self-trapped excitons and rare-earth ions was investigated.

Study of CeOx, PrOx, and CexPr1-xO2-δ films on Si(111) by means of high-energetic X-ray photoelectron spectroscopy

International Nuclear Information System (INIS)

Allahgholi, Aschkan

2013-03-01

The intention of this work is to shed light on two much discussed topics in the study of rare earth oxides (REO) by hard x-ray photoelectron spectroscopy (HAXPES): (i) Due to the complex spectral shape of the Ce3d region, there have been many discussions on proper approaches to determine the concentration of Ce 3+ and Ce 4+ species in CeO x over the last decades. (ii) Recently, the true electron structure of rare earth oxides gained new attention, since ab initio calculations showed the necessity of considering additional inter atomic charge transfer to Ce5d levels. Using HAXPES and resonant HAXPES, the question of the true electronic structure of rare earth oxides is approached from the experimental side. As a third topic, the obtained results for cerium oxide and praseodymium oxide are applied in order to investigate the plasma oxidized mixed oxide Ce x Pr 1-x O 2-δ grown on Si(111) during thermal reduction. (orig.)

Rare Earths and Clean Energy: analyzing China's upper hand

International Nuclear Information System (INIS)

Seaman, J.

2010-01-01

An ominous but avoidable resource crunch in the so-called 'rare earth elements' is now threatening the development of a number of key industries from energy to defense to consumer electronics. As key components in the latest generation of technologies, including specialized magnets for windmills and hybrid cars, lasers for range finders and 'smart' munitions, and phosphors for LCD screens, demand for these rare metals is expected to grow rapidly in the years to come. But decades of under-investment in the mining and separation of these elements across the globe has left the industry ill-prepared to meet thi s growing demand. Over the years, only China has recognized the strategic significance of these resources and has succeeded in gaining a near monopoly on production, currently churning out 97% of the world' s rare earth oxides. Faced with problems of its own, and eager to use its resource advantage to master higher levels of value-added production of rare earth-dependent products, China has increasingly limited the rest of the world's access to these raw materials. This only complicates what was already projected to be a problematic resource shortage. This issue demands a higher quality of public debate. Rare earth consuming countries outside of China have only recently become aware of their dependence and started to take stock of the risks. Time is of the essence. Bringing new supplies online to meet growing demand is a long, complicated and risky process but is nevertheless necessary to ensure the development of high tech industries, notably clean energy. Accessible reserves of rare earths do exist outside of China and mitigating the effects of the looming shortage requires opening up these reserves to production. Yet, as the Chinese experience attests, there are substantial risks to the environment associated with mining and separating rare earths. Care must be taken to ensure responsible mining practices across the globe. Longer-term solutions, such as

X-ray Absorption Spectroscopy of the Rare Earth orthophosphates

International Nuclear Information System (INIS)

Shuh, D.K.; Terminello, L.J.; Boatner, L.A.; Abraham, M.M.

1993-06-01

X-ray Absorption Spectroscopy (XAS) of the Rare Earth (RE) 3d levels yields sharp peaks near the edges as a result of strong, quasi-atomic 3d 10 4f n → 3d- 9 4f n+1 transitions and these transitions exhibit a wealth of spectroscopic features. The XAS measurements of single crystal REPO 4 (RE = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Er) at the 3d edge were performed in the total yield mode at beam line 8-2 at the Stanford Synchrotron Radiation Laboratory (SSRL). The XAS spectra of the RE ions in the orthophosphate matrix generally resemble the XAS of the corresponding RE metal. This is not unexpected and emphasizes the major contribution of the trivalent state to the electronic transitions at the RE 3d edges. These spectra unequivocally identify the transitions originating from well-characterized RE cores and correlate well with previous theoretical investigations

Redox reactions in rare earth chloride molten electrolytes

International Nuclear Information System (INIS)

Khokhlov, V.A.; Novoselova, A.V.; Nikolaeva, E.V.; Tkacheva, O.Yu.; Salyulev, A.B.

2007-01-01

Rare earth (REM, Ln) solutions in chloride melts including MCI+LnCl 3 mixtures, where M - alkali metals, were investigated by potentiometry, voltammetry, conductometry in wide concentration and temperature intervals. Findings present complete and trusty information on the valent state of rare earths, structure and composition of complex ions affecting essentially on properties of electrolytes. It is demonstrated that the coexistence of rare earth ions with different oxidation level formed as a result of possible redox reactions: 2Ln 3+ + Ln ↔3Ln 2+ , Ln 2+ + Ln↔2Ln + and nM + + Ln↔nM + Ln n+ appears sharply in thermodynamic and transport properties of molten Ln-LnCl 3 and Ln-LnCl 3 -MCl systems [ru

Reversed-phase thin-layer chromatography of the rare earth elements

International Nuclear Information System (INIS)

Kuroda, R.; Adachi, M.; Oguma, K.

1988-01-01

Partition chromatographic behaviour of the rare earth elements on C 18 bonded silica reversed-phase material has been investigated by thin-layer chromatography in methanol - lactate media. The rare earth lactato complexes are distributed and fractionated on bonded silica layers without ion-interaction reagents. The concentration and pH of lactate solution, methanol concentration and temperature have effects on the migration and resolution of the rare earth elements. The partition system is particularly suited to separate adjacent rare earths of middle atomic weight groups, allowing the separation of gadolinium, terbium, dysprosium, holmium, erbium and thulium to be achieved by development to 18 cm distance. (orig.)

Rapid separation of individual rare-earth elements from fission products

International Nuclear Information System (INIS)

Baker, J.D.; Gehrke, R.J.; Greenwood, R.C.; Meikrantz, D.H.

1980-01-01

A microprocessor-controlled radiochemical separation system has been developed to rapidly separate rare-earth elements from gross fission products. The system is composed of two high performance liquid chromatography columns coupled in series by a stream-splitting injection valve. The first column separates the rare-earth group by extraction chromatography using dihexyldiethylcarbamylmethylenephosphonate (DHDECMP) adsorbed on Vydac C 8 resin. The second column isolates the individual rare-earth elements by cation exchange using Aminex A-9 resin with α-hydroxyisobutyric acid (α-HIBA) as the eluent. With this system, fission-product rare-earth isotopes with half-lives as short as three minutes have been studied

Spectrographic determination of some rare earths in thorium compounds

International Nuclear Information System (INIS)

Brito, J. de.

1977-01-01

A method for spectrographic determination of Gd, Sm, Dy, Eu, Y, Yb, Tm and Lu in thorium compounds has been developed. Sensibilities of 0.01 μg rare earths/g Th02 were achieved. The rare earth elements were chromatographycally separated in a nitric acid-ether-cellulose system. The solvent mixture was prepared by dissolving 11% of concentrated nitric acid in ether. The method is based upon the sorption of the rare earths on activated cellulose, the elements being eluted together with 0.01 M HNO 3 . The retention of the 152 , 154 Eu used as tracer was 99,4%. The other elements showed recoveries varying from 95 to 99%. A direct carrier destillation procedure for the spectrochemical determination of the mentioned elements was used. Several concentrations of silver chloride were used to study the volatility behavior of the rare earths. 2%AgCl was added to the matrix as definite carrier, being lantanum selected as internal standard. The average coefficient of variation for this method was +- -+ 7%. The method has been appleid to the analysis of rare earths in thorium coumpounds prepared by Thorium Purification Pilot Plant at Atomic Energy Institute, Sao Paulo [pt

Enzymatic determination of rare earth elements by use of pyrophosphotases

International Nuclear Information System (INIS)

Shekhovtseva, T.N.; Pirogova, S.V.; Fedorova, O.M.; Dolmanova, I.F.; Bajkov, A.A.

1993-01-01

A highly sensitive (determination limit 8 x 10 -6 - 4 x 10 -4 μg/ml) and selective enzymatic method for determination of rare earth elements has been developed. The method is based on inhibition action of rare earths on the catalytic activity of pyrophosphates isolated from bakery geast and E. Coli. The mechanism of the rare earth element action, corresponding to competitive inhibition, has been established

Rapid analysis of some rare earth magnets

Energy Technology Data Exchange (ETDEWEB)

Raoot, K N; Raoot, S; Rukmani Desikan, N [Defence Metallurgical Research Lab., Hyderabad (India)

1978-12-01

A simple complexometric method for the quick analysis of the constituent elements in some quaternary rare earth magnets of the type RE-Co-Cu-Fe and RE-Ni-Cu-Fe is described. The technique is based on a total titration, subsequent release of EDTA from rare earth with ammonium fluoride and that from copper (II) with ascorbic acid and thiourea followed by determination of the excess and liberated EDTA by lead nitrate in a weak acid medium using xylenol orange indicator. In another, aliquot iron (III) and rare earth are first masked with sodium fluoride, and copper (II) with ascorbic acid and thiourea before cobalt (II) or nickel (II) is estimated by back titration. Iron is calculated by difference. The new method yields accurate and reproducible results with error not exceeding 1%. A set of three samples can conveniently be analysed in two hours.

Rapid analysis of some rare earth magnets

International Nuclear Information System (INIS)

Raoot, K.N.; Raoot, Sarala; Rukmani Desikan, N.

1978-01-01

A simple complexometric method for the quick analysis of the constituent elements in some quaternary rare earth magnets of the type RE-Co-Cu-Fe and RE-Ni-Cu-Fe is described. The technique is based on a total titration, subsequent release of EDTA from rare earth with ammonium fluoride and that from copper (II) with ascorbic acid and thiourea followed by determination of the excess and liberated EDTA by lead nitrate in a weak acid medium using xylenol orange indicator. In another, aliquot iron (III) and rare earth are first masked with sodium fluoride, and copper (II) with ascorbic acid and thiourea before cobalt (II) or nickel (II) is estimated by back titration. Iron is calculated by difference. The new method yields accurate and reproducible results with error not exceeding 1%. A set of three samples can conveniently be analysed in two hours. (author)

Corrosion resistance of chromium-nickel steel containing rare earths

International Nuclear Information System (INIS)

Asatiani, G.N.; Mandzhgaladze, S.N.; Tavadze, L.F.; Chuvatina, S.N.; Saginadze, D.I.

1983-01-01

Effect of additional out-of-furnace treatment with complex alloy (foundry alloy) calcite-silicon-magnesium-rare earth metal on corrosion resistance of the 03Kh18N20M3D3C3B steel has been studied. It is shown that introduction of low additions of rare earths improves its corrosion resistance improves its corrosion resistance in agressive media (in 70% - sulfuric acid) in the range of transition from active to passive state. Effect of additional introduction of rare earth metals is not considerable, if potential of steel corrosion is in the range of stable passive state (32% - sulfuric acid). Additional out-of-furnace treatment with complex foundry alloy, containing rare earth metals, provides a possibility to use a steel with a lower content of Cr, Ni, Mo, than in conventional acid-resistant steels in highly agressive media

Forced-flow chromatography of rare earths using sensitive spectrophometry

International Nuclear Information System (INIS)

Matsui, Masakazu; Aoki, Toru; Kumagai, Tetsu.

1981-01-01

The sensitive spectrophotometric method for the rare earth elements with xylenol orange in the presence of cetylpyridinium bromide was applied to the continuous detection system of liquid chromatography. Fourteen rare earth elements were completely separated within 130 min cation-exchange chromatography using 2-hydroxy-iso-butylic acid. The eluted ions were determined with absorption maxima of their complexes at around 610 nm. A linear relationship between the peak height and the amounts of rare earth elements was also obtained over the range 0.04 to 0.5 MU g. (author)

Thermochemistry of certain rare earth and ammonium double chlorides

International Nuclear Information System (INIS)

Usubaliev, D.U.; Abramtsev, V.A.; Kydynov, M.K.; Vilyaev, A.N.

1987-01-01

In a calorimeter with isothermal casing at 25 deg C dissolution enthalpies of double chlorides of rare earths and ammonium LnCl 3 x2NH 4 Cl (Ln=La, Sm) and LnCl 3 x3NH 4 Cl (Ln=Gd, Tb, Ho) in water, as well as dissolution enthalpy of rare earth chlorides in solution of ammonium chloride and NH 4 Cl in solution of rare earth chloride, have been measured. Formation enthalpies, standard formation enthalpies, dissociation enthalpies of the above-mentioned double chlorides are calculated

Separation of rare earths from solutions of phosphoric acid

International Nuclear Information System (INIS)

Jones, E.A.

1977-01-01

Rare earths are separated from 6M phosphoric acid by adsorption onto cation resin BIORAD AG50W-X8. The phosphoric acid is then washed from the column, and the rare earths are eluted with 4M hydrochloric acid

Equilibrium studies on mixed ligand complexes of some tripositive rare earth ions

International Nuclear Information System (INIS)

Vimal, Rashmi; Singh, Mamta; Ram Nayan

1996-01-01

Interaction of the rare earth ions, La 3+ , Ce 3+ , Pr 3+ , Nd 3+ , Sm 3+ and Eu 3+ with the pair of ligands 1-amino-2-naphthol-4-sulphonic acid (an, H 2 A) and o-aminophenol (ap, HB) have been studied in aqueous solution at 25 degC (μ=0.1 M KNO 3 /NaCl). Equilibrium constants of the reactions involving the formations of the mixed ligand species MAB, MA 2 B 2- , MB 2 A - (M = metal ion) and the binary complexes containing up to three ligand molecules have been evaluated from the pH-metric data, and coordinating behaviour of the ligands in the formation of the mixed ligand complexes has been discussed. (author). 10 refs., 1 tab., 1 fig

Separation of cerium from other lanthanides by leaching with nitric acid rare earth(III) hydroxide-cerium(IV) oxide mixtures

International Nuclear Information System (INIS)

Mioduski, T.; Dong Anh Hao; Hoang Hong Luan

1989-01-01

The objective of the present work is a method for separating Ce from other Ln in the raw natural mixtures of rare earth hydroxides obtained from Vietnamese and Mongolian fluorocarbonate ores. The method, a simple acid digestion, should combine a maximum Ln(III) concentration of the effluent solution with a nitrate counter-ion environment and high selectivity vs. leaching yield parameters. Under optimum conditions Ce (and Th, if present) virtually does not pass into solution while the yield of leaching and the sum of REE oxides concentration in the after-leach solution reach the maximum values of 97% (mass) and 0.18 kg x dm -3 , respectively. (author) 9 refs.; 8 tabs

Rare-earth-free high energy product manganese-based magnetic materials.

Science.gov (United States)

Patel, Ketan; Zhang, Jingming; Ren, Shenqiang

2018-06-14

The constant drive to replace rare-earth metal magnets has initiated great interest in an alternative. Manganese (Mn) has emerged to be a potential candidate as a key element in rare-earth-free magnets. Its five unpaired valence electrons give it a large magnetocrystalline energy and the ability to form several intermetallic compounds. These factors have led Mn-based magnets to be a potential replacement for rare-earth permanent magnets for several applications, such as efficient power electronics, energy generators, magnetic recording and tunneling applications, and spintronics. For past few decades, Mn-based magnets have been explored in many different forms, such as bulk magnets, thin films, and nanoparticles. Here, we review the recent progress in the synthesis and structure-magnetic property relationships of Mn-based rare-earth-free magnets (MnBi, MnAl and MnGa). Furthermore, we discuss their potential to replace rare-earth magnetic materials through the control of their structure and composition to achieve the theoretically predicted magnetic properties.

Resistivity and magnetoresistivity of amorphous rare-earth alloys

Science.gov (United States)

Borchi, E.; Poli, M.; De Gennaro, S.

1982-05-01

The resistivity and magnetoresistivity of amorphous rare-earth alloys are studied starting from the general approach of Van Peski-Tinbergen and Dekker. The random axial crystal-field and the magnetic correlations between the rare-earth ions are consistently taken into account. The characteristic features of the available experimental data are explained both of the case of random ferromagnetic and antiferromagnetic order.

Fractionation of rare earths elements in weathering profiles on phonolites in area of Lages, Santa Catarina, Brazil

International Nuclear Information System (INIS)

Formoso, M.L.L.; Valeton, J.; Retzmann, R.

1989-01-01

Niobium and rare earth elements are associated with alkaline intrusions, especially in sequences containing carbonatites. During deep ferralitic weathering on the Lower Tertiary peneplanation plain REE are mobilized and depleted as well in the lower saprolite as in the upper ferralite, except Cerium which shows a positive anormaly. Triangular diagrams of Ce, Nd, La represent a relative enrichment of La, whereas comparing Ce, La and Nb, the increase of Niobium is strongest with rising weathering. After intersection of the landscape into inselbergs and lowering of the aquifers a later period of mobilization and migration of the REE together with manganese, aluminium and silica took place in descending direction. Their absolute enrichment by precipitation is concentrated in fissure fillings and porespaces in the lowermost part of the profiles. Main minerals are lithiophorite and halloysite. (author) [pt

Determination of rare earth elements in biomonitors by neutron activation

International Nuclear Information System (INIS)

Figueiredo, Ana M.G.; Saiki, Mitiko; Ticianelli, R.B.; Domingos, M.; Alves, E.S.; Marcelli, M.P.

2000-01-01

The rare earth elements (REE) are becoming more and more important from the technological point of view, due to their increasing use in modern industry. Due to this fact, environmental contamination by REE may become significant, and little information are still available about biological effects of REE in plants, animals and human beings. The use of biomonitors to control environmental pollution has been an ecological and economical alternative in Europe and United Sates, to minimize the high costs of conventional equipment s. In the present paper, neutron activation analysis was employed to determine La, Ce, Nd, Sm, Eu, Tb, Yb and Lu in the lichen Canoparmelia texana and in Tillandsia usneoides, species that have been widely used as monitors of atmospheric pollution. The results showed an accumulation of REE in the biomonitors, indicating good possibilities of their utilization in the study of environmental contamination by REE. (author)

Behaviour of Rare Earth Elements during the Earth's core formation

Science.gov (United States)

Faure, Pierre; Bouhifd, Mohamed Ali; Boyet, Maud; Hammouda, Tahar; Manthilake, Geeth

2017-04-01

Rare Earth Elements (REE) are classified in the refractory group, which means that they have a high temperature condensation and their volatility-controlled fractionation is limited to high-temperature processes. Anomalies have been measured for Eu, Yb and Sm, which are the REE with the lowest condensation temperatures in CAIs and chondrules (e.g. [1]). REE are particularly abundant in the sulfides of enstatite chondrites, 100 to 1000 times the CI value [e.g. 2,3], proving that these elements are not strictly lithophile under extremely reducing conditions. However by investigating experimentally the impact of Earth's core formation on the behavior of Sm and Nd, we have shown the absence of fractionation between Sm and Nd during the segregation of the metallic phase [4]. Recently, Wohlers and Wood [5] proposed that Nd and Sm could be fractionated in presence of a S-rich alloy phase. However, their results were obtained at pressure and temperature conditions below the plausible conditions of the Earth's core formation. Clearly, large pressure range needs to be covered before well-constrained model can be expected. Furthermore, our preliminary metal-silicate partitioning results show that Ce and Eu have higher metal/silicate partition coefficients than their neighboring elements, and that the presence of sulphur enhances the relative difference between partition coefficients. In this presentation, we will present and discuss new metal-silicate partition coefficients of all REE at a deep magma ocean at pressures ranging from those of the uppermost upper mantle ( 5 GPa) to a maximum pressure expected in the range of 20 GPa, temperatures ranging from 2500 to about 3000 K, and oxygen fugacities within IW-1 to IW-5 (1 to 5 orders of magnitude lower than the iron-wüstite buffer). We will discuss the effect of S, as well as the effect of H2O on the behaviour of REE during the Earth's core formation: recent models suggest that contrary to currently accepted beliefs, the

Environmental Defects And Economic Impact On Global Market Of Rare Earth Metals

Science.gov (United States)

Charalampides, G.; Vatalis, K.; Karayannis, V.; Baklavaridis, A.

2016-11-01

Rare earth elements include the 14 lanthanides as well as lanthanium and often yttrium. Actually, most of them are not very rare and occur widely dispersed in a variety of rocks. Rare earth metals are vital to some of the world's faster growing industries: catalysts, Nd-magnets, ceramics, glass, metallurgy, battery alloys, electronics and phosphors. Worldwide, the main countries for distribution of rare earths deposits include China, USA, Russia, Brasil, India, Australia, Greenland and Malaysia. The mining and processing of rare earth metals usually result in significant environmental defects. Many deposits are associated with high concentrations of radioactive elements such as uranium and thorium, which requires separate treatment and disposal. The accumulation of rare earth elements in soils has occurred due to pollution caused by the exploitation of rare earth resources and the wide use of rare earths as fertilizers in agriculture. This accumulation has a toxic effect on the soil microfauna community. However, there are large differences in market prices due to the degree of purity determined by the specifications in the applications. The main focus of this article is to overview Rare Earth Metals’ overall impact on global economy and their environmental defects on soils during processing techniques and as they are used as fertilizers.

Thermal Oxidation Resistance of Rare Earth-Containing Composite Elastomer

Institute of Scientific and Technical Information of China (English)

邱关明; 张明; 周兰香; 中北里志; 井上真一; 冈本弘

2001-01-01

The rare earth-containing composite elastomer was obtained by the reaction of vinyl pyridine-SBR (PSBR) latex with rare earth alkoxides, and its thermal oxidation resistance was studied. After aging test, it is found that its retention rate of mechanical properties is far higher than that of the control sample. The results of thermogravimetric analysis show that its thermal-decomposing temperature rises largely. The analysis of oxidation mechanisms indicates that the main reasons for thermal oxidation resistance are that rare earth elements are of the utility to discontinue autoxidation chain reaction and that the formed complex structure has steric hindrance effect on oxidation.

Membrane assisted solvent extraction for rare earth element recovery

Science.gov (United States)

Bhave, Ramesh R.; Kim, Daejin; Peterson, Eric S.

2018-05-15

Systems and methods for the recovery of rare earth elements are provided. The systems and methods generally include membrane assisted solvent extraction using permeable hollow fibers having an immobilized organic phase within the pores of the hollow fibers. The permeable hollow fibers are generally in contact with an acidic aqueous feed on one side thereof and a strip solution on another side thereof. The systems and methods generally include the simultaneous extraction and stripping of rare earth elements as a continuous recovery process that is well suited for post-consumer products, end-of-life products, and other recovery sources of rare earth elements.

Thermodynamics and kinetics of the formation of rare earth intermetallics

International Nuclear Information System (INIS)

Deodhar, S.S.

1975-01-01

Heats of reaction of rare earth intermetallics with iron, cobalt and nickel were determined using Differential Thermal Analysis technique. The intermetallic compounds studied were of MgCu 2 type Laves phases and the rare earth elements studied were praseodymium, gadolinium, dyprosium and erbium. The reactions were exothermic and the heats of reaction were generally high. They varied from the low of -2.5 kcal/g mole for Fe 2 Gd to the high of -35.3 kcal/g mole for Ni 2 Er. The magnitudes of heats of reaction were always greater for the intermetallics of heavy rare earth elements. The rare earth intermetallics studied were either ferromagnetic or antiferromagnetic. The variations in the magnetic moments and the heats of reaction with respect to the atomic number of the rare earth elements followed certain trends. The similarities were observed in the trends of two properties. Electronic configuration for the MgCu 2 type rare earth intermetallics is proposed using Engel--Brewer correlation for metallic structures and the structural features of the Laves phase compounds. Kinetics of the reactions between the rare earth elements and iron, cobalt, and nickel was studied. The rate of reaction was diffusion controlled in each case. The Valensi--Carter equation for the diffusion mechanism satisfactorily described the kinetic behavior. The magnitudes of activation energies and frequency factors were determined. The reactions can be characterized by their reaction temperatures since they always begin at definite temperatures. It was observed that the reaction began at a higher temperature if the activation energy for the reaction was high

Computational search for rare-earth free hard-magnetic materials